Reaktion #73588

ord-71a0d48e151b4f408c37694c52a3b666

Reaktionsgleichung

NCc1ccc(Cl)cc1
4-chlorobenzylamine
NCc1ccccc1
benzylamine
Cc1nc(N)sc1C(=O)O
2-amino-4-methylthiazole-5-carboxylic acid
Cc1nc(N)sc1C(=O)NCc1ccc(Cl)cc1
title compound
Ausbeute 15.0%
Cc1nc(N)sc1C(=O)NCc1ccc(Cl)cc1
2-Amino-4-methylthiazole-5-carboxylic Acid 4-Chlorobenzylamide
Ausbeute 15.0%

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeas described in Preparation 1

Vorschrift

Following the procedure as described in Preparation 1, making variation only as required to use 4-chlorobenzylamine to replace benzylamine to react with 2-amino-4-methylthiazole-5-carboxylic acid, the title compound was obtained as a white solid in 15% yield; 1H NMR (CD3OD, 300 MHz) δ 7.26-7.32 (m, 4H), 4.41 (s, 2H), 2.38 (s, 3H). MS (ES+) m/z 282.1 (M+1).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541457B2uspto-grants-2013_09