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Preparation of ( R )‐3‐aminopiperidine by resolution with optically active cyclic phosphoric acids

  • Published:2021-05-03 Issue: Volume: Page:
  • ISSN:0899-0042
  • Container-title:Chirality
  • language:en
  • Short-container-title:Chirality

Author:

Sun Yujuan12ORCID,Hu Beibei12,Jing Yongshuai12,Wu Jialiang1,Zhou Maochao1,Chen Meng,Hao Feifei1,Zhang Chen3,Sun Fengxia12

Affiliation:

1. College of Chemical and Pharmaceutical Engineering Hebei University of Science and Technology Shijiazhuang China

2. Research Centre for Chemical Safety and Verification of the CWC Hebei University of Science and Technology Shijiazhuang China

3. R&D Tech Centre Hebei Chiral Chem and Biotech Co., Ltd Shijiazhuang China

Funder

Natural Science Foundation of Hebei Province

Publisher

Wiley

Subject

Organic Chemistry,Spectroscopy,Drug Discovery,Pharmacology,Catalysis,Analytical Chemistry

Reference20 articles.

1. TanH LiWP.Preparation method of alogliptin.CN.2019;109810094.

2. Synthesis of trelagliptin succinate;Xu SH;Org Process Res Dev,2017

3. Crystal forms of linagliptin intermediates;Anon;IP.com Journal,2014

4. Dielectrically controlled resolution (DCR) of 3‐aminopiper‐idine via diastereomeric salt formation with N‐Tosyl‐(S)‐phenylalanine;Sakurai R;Tetrahedron: Asymmetry,2012

5. General preparation method of optical‐activity 3‐aminopyrrolidine, 3‐alkyl amino piperidine and derivatives thereof;Yang DG;CN,2011

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