1050446-99-5

Upstream product

• 1050446-97-3 (R)-1-(p-chlorobenzoyl)nipecotamide 

Downstream Products

• 1050447-05-6 (R)-1-(p-chlorobenzoyl)-3-(p-chlorobenzoylamino) piperidine 
• 1050447-01-2 (R)-1-(p-chlorolbenzoyl)-3-(benzoylamino)piperidine 
• 1050447-07-8 (R)-1-(p-chlorobenzoyl)-3-(tert-butoxycarbonylamino)piperidine 
• 1050447-09-0 (R)-1-(p-chlorobenzoyl)-3-(benzyloxycarbonylamino)piperidine 
• 1050447-03-4 (R)-1-(p-chlorolbenzoyl)-3-(p-methylbenzoylamino)piperidine 

Relevant academic research and scientific papers

METHOD FOR PRODUCING OPTICALLY ACTIVE 3-AMINOPIPERIDINE OR SALT THEREOF

The present invention relates to a method for producing an optically active 3-aminopiperidine or salt thereof. In the method, a racemic nipecotamide is stereoselectively hydrolyzed to obtain an optically active nipecotamide and an optically active nipecotic acid in the presence of an enzyme source derived from an organism, and then the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by aroylation, Hofmann rearrangement, deprotection of the amino group and further deprotection; or the optically active nipecotamide is derived into an optically active aminopiperidine or salt thereof by selective protection with BOC, Hofmann rearrangement and further deprotection. It is possible by the present invention to produce an optically active 3-aminopiperidine or salt thereof useful as a pharmaceutical intermediate from an inexpensive and easily available starting material by easy method applicable to industrial manufacturing.