Piramal Pharma Limited

Sharadsrikar Kotturi

Chirag Patel

Rajender Reddy Leleti

Yogesh Waman

Vinkal Zalavadiya

Kumara Swamy Nalivela

Rajesh Shenoy

Ramesh Babu Bandi

Manoj Kumar Mandadi

Venkataramana Rao Rao

Krishna Nayak

Thumban Divya

Kasimraza Baharooni

Abdul Basith

Paranjay Parikh

Zubeda Begum

Poojabahen Raval

Priya Kallure

Saurabh Vijay

Aditya Patwa

The present invention relates to an improved process for the preparation of N-((1R,2R)-1-(2,3-dihydrobenzo[b][1,4]dioxin-6-yl)-1-hydroxy-3-(pyrrolidin-1-yl)propan-2-yl)octanamide (A), which is known as ELIGLUSTAT and its pharmaceutically acceptable salts, comprising the formation of novel intermediate metal complex (III), which on hydrolysis in presence of acid provides amine compound (IV) (as described herein), which is treated with pyrrolidine and subsequently reduced to convert into Eliglustat (A).

Process for the preparation of ELIGLUSTAT and its intermediate

The present invention relates to an improved asymmetric synthesis of azaspiro or diazaspiro compound (hereafter referred to as the compound 5, (5) or (5)) or their pharmaceutically acceptable salts and derivatives; through the formation of intermediate compounds 4, (4) or (4) respectively. The process comprises an unusual substrate specific highly diastereoselective as well as enantio-enriched 1-substituted 2-azaspiro[3.3]heptane or 1-substituted 2-diazaspiro[3.3]heptane compounds with high diastereoselectivity by addition of a cyclobutane carboxylate anion to a Davis-Ellman's imine, followed by reduction and cyclisation resulting in the selective formation of azaspiro or diazaspiro intermediate compound 4, (4) or (4); which on subsequently removing the sulfinyl group provides corresponding azaspiro or diazaspiro compound 5, (5) or (5) respectively.

Asymmetric synthesis of Azaspiro compounds

The present invention relates to an improved process for diastereoselective synthesis of vicinal diamines (1). The process involves highly regio- and diastereoselective addition of 2-azaallyl anions (4) to N-tert-butanesulfinylimines (5) to produce vicinal diamines (1).

Process for diastereoselective synthesis of vicinal diamines

The present invention relates to an improved asymmetric synthesis of alpha-(diarylmethyl) alkyl amines (hereafter referred to as the compound (1)) or its pharmaceutically acceptable salt and derivatives. The process comprises an unusual substrate specific regioselective lithiation of alpha-diarylmethanes. followed by its highly diastereoselective addition to N-tert-butanesulfinylimines resulting in the selective formation of chiral alpha-(diarylmethyl) alkyl amines 4 and chiral amine 5; which on subsequently removing the sulfinyl group provides corresponding alpha-(diarylmethyl) alkyl amines (1) or relative chiral amines (1&#x2033;).

Asymmetric synthesis of alpha-(diarylmethyl) alkyl amines

The present invention relates to an improved asymmetric synthesis of alpha-branched amines (hereafter referred to as the compound) and relative chiral amines (1&#x2033;) or its pharmaceutically acceptable salt and derivatives. The process comprises an unusual substrate specific regioselective ortho lithiation of substituted arene compounds, followed by its highly diastereoselective addition to N-tert-butanesulfinylimines resulting in the selective formation of alpha-branched sulfinyl amine and chiral amine; which on subsequently removing the sulfinyl group provides corresponding alpha-branched amines or relative chiral amines (1&#x2033;).

Asymmetric synthesis of alpha-branched chiral amines

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Gujarat, India

Sharadsrikar Kotturi