Substituted triazolo[1,5-a]pyridines and triazolo[1,5-a]pyrazines as LSD1 inhibitors

• US 9,695,167 B2
• Filed: 07/09/2015
• Issued: 07/04/2017
• Est. Priority Date: 07/10/2014
• Status: Active Grant

• Current Assignee: Incyte Corporation, Incyte Holdings Corporation (Incyte Corporation)
• Original Assignee: Incyte Corporation
• Inventors: Zhang, Colin, Wang, Xiaozhao, Yao, Wenqing, Wu, Liangxing
• Primary Examiner(s): Willis, Douglas M
• Application Number:
  US14/795,499
• Publication Number:
  US 20160009711A1
• Time in Patent Office: 726 Days
• Field of Search: 514249, 514303, 544350, 546119
• CPC Class Codes: A61P 35/00 Antineoplastic agents
• CPC Class Codes: C07D 471/04 Ortho-condensed systems
• CPC Class Codes: C07D 487/04 Ortho-condensed systems

Abstract

The present invention is directed to [1,2,4]triazolo[1,5-a]pyridine and [1,2,4]triazolo[1,5-a]pyrazine derivatives of Formula I, or a pharmaceutically acceptable salt thereof, which are LSD1 inhibitors useful in the treatment of diseases such as cancer.

Claims

1. A compound of Formula I:

2. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein:

X is N or CR^X;

Ring A is phenyl or 5-10 membered heteroaryl comprising carbon and 1, 2, 3, or 4 heteroatoms selected from N, O, and S, wherein said C_6-10 aryl and 5-10 membered heteroaryl are each optionally substituted by 1, 2, 3, or 4 substituents independently selected from R^A;

Ring B is phenyl or 5-6 membered heteroaryl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from N, O, and S;

wherein said phenyl and 5-6 membered heteroaryl are each optionally substituted by 1, 2, 3, or 4 substituents independently selected from R^B;

R¹ is halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, Cy¹, CN, OR^a1, SR^a1, C(O)R^b1, C(O)NR^c1R^d1, C(O)OR^a1, OC(O)R^b1, OC(O)NR^c1R^d1, NR^c1R^d1, NR^c1C(O)R^b1, NR^c1C(O)OR^a1, NR^c1C(O)NR^c1R^d1, C(═

NR^e1)R^b1, C(═

NR^e1)NR^c1R^d1, NR^c1C(═

NR^e1)NR^c1R^d1, NR^c1S(O)R^b1, NR^c1S(O)₂R^b1, NR^c1S(O)₂NR^c1R^d1, S(O)R^b1, S(O)NR^c1R^d1, S(O)₂R^b1, or S(O)₂NR^c1R^d1;

wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy¹, halo, CN, OR^a1, SR^a1, C(O)R^b1, C(O)NR^c1R^d1, C(O)OR^a1, OC(O)R^b1, OC(O)NR^c1R^d1, NR^c1R^d1, NR^c1C(O)R^b1, NR^c1C(O)OR^a1, NR^c1C(O)NR^c1R^d1, C(═

NR^e1)R^b1, C(═

NR^e1)R^c1R^d1, NR^c1C(═

NR^e1)NR^c1R^d1, NR^c1S(O)R^b1, NR^c1S(O)₂R^b1, NR^c1S(O)₂NR^c1R^d1, S(O)R^b1, S(O)NR^c1R^d1, S(O)₂R^b1, and S(O)₂NR^c1R^d1;

wherein when X is CR^X, then R¹ is not CN;

R² is H, halo, C_1-6 alkyl, CN, OR^a2, C(O)R^b2, C(O)NR^c2R^d2, NR^c2R^d2 NR^c2C(O)R^b2, S(O)₂R^b2, or S(O)₂NR^c2R^d2;

wherein said C_1-6 alkyl is optionally substituted with 1, 2, or 3 substituents independently selected from halo, CN, OR^a2, C(O)R^b2, C(O)NR^c2R^d2, NR^c2R^d2, NR^c2C(O)R^b2, S(O)₂R^b2, and S(O)₂NR^c2R^d2;

each R^A is independently selected from halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, OR^a4, C(O)R^b4, C(O)NR^c4R^d4, C(O)OR^a4, NR^c4R^d4, NR^c4C(O)R^b4, S(O)₂R^b4, and S(O)₂NR^c4R^d4, wherein said C_1-6 alkyl is optionally substituted by 1, 2, or 3, substituents independently selected from halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, OR^a4, C(O)R^b4, C(O)NR^c4R^d4, C(O)OR^a4, NR^c4R^d4, NR^c4C(O)R^b4, S(O)₂R^b4, and S(O)₂NR^c4R^d4;

each R^B is independently selected from Cy³, halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, CN, NO₂, OR^a5, C(O)R^b5, C(O)NR^c5R^d5, C(O)OR^a5, NR^c5R^d5, NR^c5C(O)R^b5, S(O)₂R^b5, and S(O)₂NR^c5R^d5, wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted by 1, 2, or 3 substituents independently selected from Cy³, halo, C_1-6 haloalkyl, CN, NO₂, OR^a5, C(O)R^b5, C(O)NR^c5R^d5, C(O)OR^a5, NR^c5R^d5, NR^c5C(O)R^b5, S(O)₂R^b5, and S(O)₂NR^c5R^d5;

R^X is independently selected from H, halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, OR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, NR^c7R^d7, NR^c7C(O)R^b7, S(O)₂R^b7, and S(O)₂NR^c7R^d7;

each Cy¹, Cy³, and Cy⁴ is independently selected from C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, and 4-10 membered heterocycloalkyl, each of which is optionally substituted with 1, 2, 3, or 4 substituents independently selected from R^Cy;

each R^Cy is independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, C_2-6 alkenyl, C_2-6 alkynyl, phenyl, C_3-7 cycloalkyl, 5-6 membered heteroaryl, 4-7 membered heterocycloalkyl, phenyl-C_1-4 alkyl-, C_3-7 cycloalkyl-C_1-4 alkyl-, (5-6 membered heteroaryl)-C_1-4 alkyl-, and (4-7 membered heterocycloalkyl)-C_1-4 alkyl-, CN, NO₂, OR^a6, SR^a6, C(O)R^b6, C(O)NR^c6R^d6, C(O)OR^a6, OC(O)R^b6, OC(O)NR^c6R^d6, C(═

NR^e6)NR^c6R^d6, NR^c6C(═

NR^e6)NR^c6R^d6, NR^c6R^d6, NR^c6C(O)R^b6, NR^c6C(O)OR^a6, NR^c6C(O)NR^c6R^d6, NR^c6S(O)R^b6, NR^c6S(O)₂R^b6, NR^c6S(O)₂NR^c6R^d6, S(O)R^b6, S(O)NR^c6R^d6, S(O)₂R^b6, and S(O)₂NR^c6R^d6, wherein said C_1-4 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, phenyl, C_3-7 cycloalkyl, 5-6 membered heteroaryl, 4-7 membered heterocycloalkyl, phenyl-C_1-4 alkyl-, C_3-7 cycloalkyl-C_1-4 alkyl-, (5-6 membered heteroaryl)-C_1-4 alkyl-, and (4-7 membered heterocycloalkyl)-C_1-4 alkyl- are each optionally substituted by 1, 2, or 3 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, NO₂, OR^a6, SR^a6, C(O)R^b6, C(O)NR^c6R^d6, C(O)OR^a6, OC(O)R^b6, OC(O)NR^c6R^d6, C(═

NR^e6)NR^c6R^d6, NR^c6C(═

NR^e6)NR^c6R^d6, NR^c6R^d6, NR^c6C(O)R^b6, NR^c6C(O)OR^a6, NR^c6C(O)NR^c6R^d6, NR^c6S(O)R^b6, NR^c6S(O)₂R^b6, NR^c6S(O)₂NR^c6R^d6, S(O)R^b6, S(O)NR^c6R^d6, S(O)₂R^b6, and S(O)₂NR^c6R^d6;

each R^a1 is independently selected from H, C_1-6 alkyl, and Cy⁴;

wherein said C_1-6 alkyl is optionally substituted with 1, 2, or 3 substituents independently selected from Cy⁴, halo, CN, OR^a3, C(O)R^b3, C(O)NR^c3R^d3, C(O)OR^a3, NR^c3R^d3, NR^c3C(O)R^b3, S(O)₂R^b3, and S(O)₂NR^c3R^d3;

each R^b1, R^c1, and R^d1 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl-, wherein said C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl- are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

or any R^c1 and R^d1 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C_6-10 aryl, 5-6 membered heteroaryl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7, wherein said C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C_6-10 aryl, and 5-6 membered heteroaryl are each optionally substituted by 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^cR^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

each R^a2, R^b2, R^c2, and R^d2 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl-, wherein said C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl- are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^cR^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

or any R^c2 and R^d2 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, phenyl, 5-6 membered heteroaryl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^cR^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7, wherein said C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, phenyl, and 5-6 membered heteroaryl are each optionally substituted by 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^cR^d7, and S(O)₂NR^c7R^d7;

each R^a3, R^b3, R^c3, and R^d3 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl-, wherein said C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl- are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7 NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7 and S(O)₂NR^c7R^d7;

or any R^c3 and R^d3 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, phenyl, 5-6 membered heteroaryl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7 NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7 NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7, wherein said C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, phenyl, and 5-6 membered heteroaryl are each optionally substituted by 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^cR^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^cR^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

each R^a4, R^b4, R^c4, and R^d4 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, and C_2-6 alkynyl, wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7 NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

or any R^c4 and R^d4 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7 NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

each R^a5, R^b5, R^c5, and R^d5 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl-, wherein said C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_6-10 aryl, C_3-10 cycloalkyl, 5-10 membered heteroaryl, 4-10 membered heterocycloalkyl, C_6-10 aryl-C_1-4 alkyl-, C_3-10 cycloalkyl-C_1-4 alkyl-, (5-10 membered heteroaryl)-C_1-4 alkyl-, and (4-10 membered heterocycloalkyl)-C_1-4 alkyl- are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, R^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

or any R^c5 and R^d5 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C_6-10 aryl, 5-6 membered heteroaryl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7, wherein said C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C_6-10 aryl, and 5-6 membered heteroaryl are each optionally substituted by 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7 NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7, NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

each R^a6, R^b6, R^c6, and R^d6 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, and C_2-6 alkynyl, wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7 NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7 NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

or any R^c6 and R^d6 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7 NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7 NR^c7C(O)OR^a7, C(═

NR^e7)NR^c7R^d7, NR^c7C(═

NR^e7)NR^c7R^d7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

each R^a7, R^b7, R^c7, and R^d7 is independently selected from H, C_1-4 alkyl, C_1-4 haloalkyl, C_2-4 alkenyl, and C_2-4 alkynyl, wherein said C_1-4 alkyl, C_2-4 alkenyl, and C_2-4 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from OH, CN, amino, halo, C_1-4 alkyl, C_1-4 alkoxy, C_1-4 alkylthio, C_1-4 alkylamino, di(C_1-4 alkyl)amino, C_1-4 haloalkyl, and C_1-4 haloalkoxy; and

each R^e1, R^e6, and R^e7 is independently selected from H, C_1-4 alkyl, and CN.

3. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein:

X is N or CR^X;

Ring A is phenyl optionally substituted by 1 or 2 substituents independently selected from R^A;

Ring B is phenyl optionally substituted by 1 or 2 substituents independently selected from R^B;

R¹ is halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, Cy¹, OR^a1, C(O)R^b1, C(O)NR^c1R^d1, C(O)OR^a1, NR^c1R^d1, NR^c1C(O)R^b1, NR^c1C(O)OR^a1, S(O)₂R^b1, or S(O)₂NR^c1R^d1;

wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy¹, halo, CN, OR^a1, C(O)R^b1, C(O)NR^c1R^d1, C(O)OR^a1, NR^c1R^d1, NR^c1C(O)R^b1, S(O)₂R^b1, and S(O)₂NR^c1R^d1;

R² is H;

each R^A is independently selected from halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, and OR^a4, wherein said C_1-6 alkyl is optionally substituted by 1, 2, or 3, substituents independently selected from CN and OR^a4;

each R^B is independently selected from halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, CN, and OR^a5;

R^X is H;

each Cy¹ and Cy⁴ is independently selected from phenyl, C_3-7 cycloalkyl, 5-6 membered heteroaryl, and 4-7 membered heterocycloalkyl, each of which is optionally substituted with 1, 2, 3, or 4 substituents independently selected from R^Cy;

each R^Cy is independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, C_2-6 alkenyl, C_2-6 alkynyl, CN, NO₂, OR^a6, SR^a6, C(O)R^b6, C(O)NR^c6R^d6, C(O)OR^a6, OC(O)R^b6, OC(O)NR^c6R^d6, NR^c6R^d6, NR^c6C(O)R^b6, NR^c6C(O)OR^a6, NR^c6C(O)NR^c6R^d6, NR^c6S(O)R^b6, NR^c6S(O)₂R^b6, NR^c6S(O)₂NR^c6R^d6, S(O)R^b6, S(O)NR^c6R^d6, S(O)₂R^b6, and S(O)₂NR^c6R^d6, wherein said C_1-4 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, are each optionally substituted by 1, 2, or 3 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, NO₂, OR^a6, SR^a6, C(O)R^b6, C(O)NR^c6R^d6, C(O)OR^a6, OC(O)R^b6, OC(O)NR^c6R^d6, NR^c6R^d6, NR^c6C(O)R^b6, NR^c6C(O)OR^a6, NR^c6C(O)NR^c6R^d6, NR^c6S(O)R^b6, NR^c6S(O)₂R^b6, NR^c6S(O)₂NR^c6R^d6, S(O)R^b6, S(O)NR^c6R^d6, S(O)₂R^b6, and S(O)₂NR^c6R^d6;

each R^a1 is independently selected from H, C_1-6 alkyl, and 4-7 membered heterocycloalkyl;

wherein said C_1-6 alkyl is optionally substituted with 1, 2, or 3 substituents independently selected from Cy⁴, halo, CN, OR^a3, C(O)R^b3, C(O)NR^c3R^d3, C(O)OR^a3, NR^c3R^d3, NR^c3C(O)R^b3, S(O)₂R^b3, and S(O)₂NR^c3R^d3, and wherein said 4-7 membered heterocycloalkyl is optionally substituted with 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, NO₂, OR^a6, C(O)R^b6, C(O)NR^c6R^d6, C(O)OR^a6, NR^c6R^d6, NR^c6C(O)R^b6, S(O)₂R^b6, and S(O)₂NR^c6R^d6;

each R^b1, R^c1, and R^d1 is independently selected from H, C_1-6 alkyl, C_1-4 haloalkyl, C_2-6 alkenyl, C_2-6 alkynyl, phenyl, C_3-7 cycloalkyl, 5-6 membered heteroaryl, 4-7 membered heterocycloalkyl, phenyl-C_1-4 alkyl-, C_3-7 cycloalkyl-C_1-4 alkyl-, (5-6 membered heteroaryl)-C_1-4 alkyl-, and (4-7 membered heterocycloalkyl)-C_1-4 alkyl-, wherein said C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, phenyl, C_3-7 cycloalkyl, 5-6 membered heteroaryl, 4-7 membered heterocycloalkyl, phenyl-C_1-4 alkyl-, C_3-7 cycloalkyl-C_1-4 alkyl-, (5-6 membered heteroaryl)-C_1-4 alkyl-, and (4-7 membered heterocycloalkyl)-C_1-4 alkyl- are each optionally substituted with 1, 2, 3, 4, or 5 substituents independently selected from C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^cR^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^c7R^d7 NR^c7C(O)OR^a7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

or any R^c1 and R^d1 together with the N atom to which they are attached form a 4-, 5-, 6-, or 7-membered heterocycloalkyl group optionally substituted with 1, 2, or 3 substituents independently selected from C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C_6-10 aryl, 5-6 membered heteroaryl, C_1-6 haloalkyl, halo, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7 NR^c7C(O)R^b7, NR^c7C(O)NR^cR^d7, NR^c7C(O)OR^a7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7, wherein said C_1-6 alkyl, C_3-7 cycloalkyl, 4-7 membered heterocycloalkyl, C_6-10 aryl, and 5-6 membered heteroaryl are each optionally substituted by 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, OR^a7, SR^a7, C(O)R^b7, C(O)NR^c7R^d7, C(O)OR^a7, OC(O)R^b7, OC(O)NR^c7R^d7, NR^c7R^d7, NR^c7C(O)R^b7, NR^c7C(O)NR^cR^d7, NR^c7C(O)OR^a7, S(O)R^b7, S(O)NR^c7R^d7, S(O)₂R^b7, NR^c7S(O)₂R^b7, NR^c7S(O)₂NR^c7R^d7, and S(O)₂NR^c7R^d7;

each R^a3, R^b3, R^c3, and R^d3 is independently selected from H and C_1-6 alkyl;

each R^a4 is independently selected from H and C_1-6 alkyl;

each R^a5 is independently selected from H and C_1-6 alkyl;

each R^a6, R^b6, R^c6, and R^d6 is independently selected from H and C_1-6 alkyl; and

each R^a7, R^b7, R^c7, and R^d7 is independently selected from H and C_1-4 alkyl.

4. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein X is N.

5. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein X is CR^X.

6. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R^X is H.

7. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring A is phenyl or 5-10 membered heteroaryl comprising carbon and 1, 2, 3, or 4 heteroatoms selected from N, O, and S, wherein said phenyl and 5-10 membered heteroaryl are each optionally substituted by 1, 2, 3, or 4 substituents independently selected from R^A.

8. The compound of claim 1 or claim 2, or a pharmaceutically acceptable salt thereof, wherein Ring A is phenyl optionally substituted by 1 or 2 substituents independently selected from R^A.

9. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring A is phenyl substituted by one R^A.

10. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring A is phenyl substituted by CN.

11. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring B is phenyl or 5-6 membered heteroaryl comprising carbon and 1, 2, 3 or 4 heteroatoms selected from N, O, and S;

wherein said phenyl and 5-6 membered heteroaryl are each optionally substituted by 1, 2, 3, or 4 substituents independently selected from R^B.

12. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring B is phenyl optionally substituted by 1 or 2 substituents independently selected from R^B.

13. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring B is phenyl substituted by one R^B.

14. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein Ring B is phenyl substituted by CH₃.

15. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^A is independently selected from halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, OR^a4, C(O)R^b4, C(O)NR^c4R^d4, C(O)OR^a4, NR^c4R^d4, NR^c4C(O)R^b4, S(O)₂R^b4, and S(O)₂NR^c4R^d4, wherein said C_1-6 alkyl is optionally substituted by 1, 2, or 3, substituents independently selected from halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, OR^a4, C(O)R^b4, C(O)NR^c4R^d4, C(O)OR^a4, NR^c4R^d4, NR^c4C(O)R^b4, S(O)₂R^b4, and S(O)₂NR^c4R^d4.

16. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^A is independently selected from halo, C_1-6 alkyl, C_1-6 haloalkyl, CN, and OR^a4, wherein said C_1-6 alkyl is optionally substituted by 1, 2, or 3, substituents independently selected from CN and OR^a4.

17. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R^A is CN.

18. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^B is independently selected from Cy³, halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, CN, NO₂, OR^a5, C(O)R^b5, C(O)NR^c5R^d5, C(O)OR^a5, NR^c5R^d5, NR^c5C(O)R^b5, S(O)₂R^b5, and S(O)₂NR^c5R^d5, wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted by 1, 2, or 3 substituents independently selected from Cy³, halo, C_1-6 haloalkyl, CN, NO₂, OR^a5, C(O)R^b5, C(O)NR^c5R^d5, C(O)OR^a5, NR^c5R^d5, NR^c5C(O)R^b5, S(O)₂R^b5, and S(O)₂NR^c5R^d5.

19. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^B is independently selected from halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, CN, and OR^a5.

20. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R^B is C_1-6 alkyl.

21. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R^B is CH₃.

22. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R¹ is halo, C_1-6 alkyl, C_2-6 alkenyl, C_2-6 alkynyl, C_1-6 haloalkyl, Cy¹, OR^a1, C(O)R^b1, C(O)NR^c1R^d1, C(O)OR^a1, NR^c1R^d1, NR^c1C(O)R^b1, NR^c1C(O)OR^a1, S(O)₂R^b1, or S(O)₂NR^c1R^d1;

wherein said C_1-6 alkyl, C_2-6 alkenyl, and C_2-6 alkynyl are each optionally substituted with 1, 2, or 3 substituents independently selected from Cy¹, halo, CN, OR^a1, C(O)R^b1, C(O)NR^c1R^d1, C(O)OR^a1, NR^c1R^c1, NR^c1C(O)R^b1, S(O)₂R^b1, and S(O)₂NR^c1R^d1.

23. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R¹ is C_1-6 alkyl, Cy¹, or OR^a1, wherein said C_1-6 alkyl is substituted by one Cy¹.

24. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R¹ is pyrrolidin-3-ylmethoxy, 2-pyrrolidin-3-ylethyl, (1-methylpyrrolidin-3-yl)ethyl, 3-[(methylamino)methyl]phenyl, 3-aminopyrrolidin-1-yl)methyl]phenyl, piperazin-1-ylmethyl, 4-methylpiperazin-1-yl)methyl, 3-(dimethylamino)pyrrolidin-1-yl, 3-(methylamino)pyrrolidin-1-yl, or (1-methylpyrrolidin-3-yl)methoxy.

25. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R² is H.

26. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each Cy¹ is independently selected from phenyl, C_3-7 cycloalkyl, 5-6 membered heteroaryl, and 4-7 membered heterocycloalkyl, each of which is optionally substituted with 1, 2, 3, or 4 substituents independently selected from R.

27. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each Cy¹ is phenyl or 4-7 membered heterocycloalkyl, each optionally substituted with 1 or 2 substituents independently selected from R.

28. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each Cy¹ is phenyl, pyrrolidinyl, or piperazinyl, each optionally substituted with 1 or 2 substituents independently selected from R^Cy.

29. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each Cy¹ is phenyl, pyrrolidinyl, or piperazinyl, each optionally substituted with 1 or 2 substituents independently selected from C_1-4 alkyl and NR^c6R^d6, wherein said C_1-4 alkyl is optionally substituted with NR^c6R^d6.

30. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein R^Cy is C_1-4 alkyl and NR^c6R^d6, wherein said C_1-4 alkyl is optionally substituted with NR^c6R^d6.

31. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^a1 is independently selected from H, C_1-6 alkyl, and Cy⁴;

wherein said C_1-6 alkyl is optionally substituted with 1, 2, or 3 substituents independently selected from Cy⁴, halo, CN, OR^a3, C(O)R^b3, C(O)NR^c3R^d3, C(O)OR^a3, NR^c3R^d3, NR^c3C(O)R^b3, S(O)₂R^b3, and S(O)₂NR^c3R^d3.

32. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^a1 is independently selected from H, C_1-6 alkyl, and 4-7 membered heterocycloalkyl;

wherein said C_1-6 alkyl is optionally substituted with 1, 2, or 3 substituents independently selected from Cy⁴, halo, CN, OR^a3, C(O)R^b3, C(O)NR^c3R^d3, C(O)OR^a3, NR^c3R^d3, NR^c3C(O)R^b3, S(O)₂R^b3, and S(O)₂NR^c3R^d3, and wherein said 4-7 membered heterocycloalkyl is optionally substituted with 1, 2, or 3 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, NO₂, OR^a6, C(O)R^b6, C(O)NR^c6R^d6, C(O)OR^a6, NR^c6R^d6, NR^c6C(O)R^b6, S(O)₂R^b6, and S(O)₂NR^c6R^d6.

33. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^a1 is C_1-4 alkyl substituted by 4-7 membered heterocycloalkyl, wherein said 4-7 membered heterocycloalkyl is optionally substituted with 1 or 2 substituents independently selected from halo, C_1-4 alkyl, C_1-4 haloalkyl, C_1-4 cyanoalkyl, CN, NO₂, OR^a6, C(O)R^v6, C(O)NR^c6R^d6, C(O)OR^a6, NR^c6R^d6, NR^c6C(O)R^b6, S(O)₂R^b6, and S(O)₂NR^c6R^d6.

34. The compound of claim 1, or a pharmaceutically acceptable salt thereof, wherein each R^a1 is pyrrolidinylmethyl optionally substituted by one C_1-4 alkyl.

35. The compound of claim 1 having Formula IIa:

36. The compound of claim 1 having Formula IIb:

37. The compound of claim 1 having Formula IIIa:

38. The compound of claim 1 having Formula IIIb:

39. The compound of claim 1 selected from:

4-{5-(4-methylphenyl)-8-[(3R)-pyrrolidin-3-ylmethoxy][1,2,4]triazolo[1,5-a]pyridin-6-yl}benzonitrile;

4-[5-(4-methylphenyl)-8-(2-pyrrolidin-3-ylethyl)[1,2,4]triazolo[1,5-a]pyridin-6-yl]benzonitrile;

4-{5-(4-methylphenyl)-8-[2-(1-methylpyrrolidin-3-yl)ethyl][1,2,4]triazolo[1,5-a]pyridin-6-yl}benzonitrile;

4-[8-{3-[(methylamino)methyl]phenyl}-5-(4-methylphenyl)[1,2,4]triazolo[1,5-a]pyridin-6-yl]benzonitrile;

4-[8-{3-[(3-aminopyrrolidin-1-yl)methyl]phenyl}-5-(4-methylphenyl)[1,2,4]triazolo[1,5-a]pyridin-6-yl]benzonitrile;

4-[5-(4-methylphenyl)-8-(piperazin-1-ylmethyl)[1,2,4]triazolo[1,5-a]pyridin-6-yl]benzonitrile;

4-{5-(4-methylphenyl)-8-[(4-methylpiperazin-1-yl)methyl][1,2,4]triazolo[1,5-a]pyridin-6-yl}benzonitrile;

4-[8-{[(3 S)-3-(dimethylamino)pyrrolidin-1-yl]methyl}-5-(4-methylphenyl)-[1,2,4]triazolo-[1,5-a]pyridin-6-yl]benzonitrile;

4-[8-{[(3R)-3-(dimethylamino)pyrrolidin-1-yl]methyl}-5-(4-methylphenyl)-[1,2,4]triazolo-[1,5-a]pyridin-6-yl]benzonitrile;

4-[8-{[(3 S)-3-(methylamino)pyrrolidin-1-yl]methyl}-5-(4-methylphenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]benzonitrile;

4-[8-{[(3R)-3-(methylamino)pyrrolidin-1-yl]methyl}-5-(4-methylphenyl)-[1,2,4]triazolo[1,5-a]pyridin-6-yl]benzonitrile;

4-{5-(4-methylphenyl)-8-[(3R)-pyrrolidin-3-ylmethoxy][1,2,4]triazolo[1,5-a]pyrazin-6-yl}benzonitrile; and

4-(5-(4-methylphenyl)-8-{[(3R)-1-methylpyrrolidin-3-yl]methoxy}[1,2,4]triazolo[1,5-a]pyrazin-6-yl)benzonitrile,

or a pharmaceutically acceptable salt of any of the aforementioned.

40. A pharmaceutical composition comprising a compound of claim 1, or a pharmaceutically acceptable salt thereof, and at least one pharmaceutically acceptable carrier.

41. A method of inhibiting lysine specific demethylase-1 comprising contacting a compound of claim 1, or a pharmaceutically acceptable salt thereof, with said lysine specific demethylase-1.