Solid .alpha.-phenyl-2-piperidine acetate free base, its preparation and use in medicine

• US 6,096,760 A
• Filed: 05/29/1998
• Issued: 08/01/2000
• Est. Priority Date: 05/30/1997
• Status: Expired due to Term

• Current Assignee: Johnson Matthey PLC
• Original Assignee: Johnson Matthey PLC
• Inventors: Sapino, Chester
• Primary Examiner(s): CHANG, CELIA C
• Application Number:
  US09/086,727
• Time in Patent Office: 795 Days
• Field of Search: 514/317, 514/331, 546/233
• US Class Current: 514/317
• CPC Class Codes: A61K 9/7023 Transdermal patches and similar drug-containing composite devices, e.g. cataplasms galenical aspects of iontophoretic devices A61K9/0009; microneedle arrays A61K9/0021; buccal patches A61K9/006
• CPC Class Codes: A61P 25/26 Psychostimulants, e.g. nicotine, cocaine
• CPC Class Codes: C07D 211/34 with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals

Abstract

Methyl α-phenyl-2-piperidine acetate (free base) is disclosed as a crystalline solid, together with a method for its preparation; its use in medicine, in particular as a stimulant for the central nervous system; and pharmaceutical formulations comprising the compound, particularly transdermal patches.

Claims

1. The compound methyl α

-phenyl-2-piperidine acetate free base, in solid form and having a melting point of 41-42°

C.

2. The compound of claim 1, in crystalline form.

3. A method of stimulating the central nervous system in a patient in need thereof, which method comprises the administration to the patient of a therapeutically effective amount of a compound according to claim 1 or claim 2.

4. A pharmaceutical formulation comprising a compound according to claim 1 or claim 2, together with a pharmaceutically acceptable carrier therefor.

5. A pharmaceutical formulation comprising a compound according to claim 1 or claim 2 in a form selected from those suitable for topical and transdermal administration.

6. A transdermal patch, comprising a compound according to claim 1 or claim 2.

7. A process for preparing a compound according to claim 1 or claim 2, which process comprises the steps of:

(i) dissolving a salt of methyl α

-phenyl-2-piperidine acetate hydrochloride in a mixture of a suitable organic solvent and an aqueous base; and

(ii) evaporating the organic solution from the aqueous solution thereby formed, whereby an oil is formed that solidifies on standing to form crude solid free base.

8. A process for preparing a compound according to claim 1 or claim 2, which process comprises the steps of:

(i) dissolving a salt of methyl α

-phenyl-2-piperidine acetate hydrochloride in a mixture of a suitable organic solvent and an aqueous base;

(ii) evaporating the organic solution from the aqueous solution thereby formed, whereby an oil is formed that solidifies on standing to form crude solid free base, dissolving the crude solid, obtained from steps (i) to (ii), in an organic solvent and recrystallising the free base therefrom; and

(iii) dissolving the crude solid, obtained from steps (i) to (ii), in an organic solvent and recrystallising the free base therefrom.

9. A process for preparing methyl α

-phenyl-2-piperidine acetate (free base), which process comprises the steps of;

(i) stirring methyl α

-phenyl-2-piperidine acetate hydrochloride in a suitable organic solvent and aqueous base;

(ii) evaporating the organic layer to leave an oil which solidifies on standing; and

(iii) dissolving the crude solid in an organic solvent, cooling to less than 10°

C. and seeding with crude solid whilst continuing stirring.

10. A process according to claim 9, which process comprises:

(i) stirring methyl α

-phenyl-2-piperidine acetate hydrochloride in heptane and an aqueous inorganic base, such as an alkali or alkaline earth metal hydroxide or carbonate;

(ii) evaporating the solvent from the organic layer to leave an oil that solidifies on standing; and

, optionally,

(iii) dissolving the crude solid in 2,2,4-trimethylpentane, and seeding with crude solid at below 10°

C. with stirring.