تفاعل #73636

ord-67e90ad412c9495b9d57483c574bfd58

معادلة التفاعل

COc1cccc(C(=O)Cl)c1
3-methoxybenzoyl chloride
Cc1nc(N)sc1C(=O)NCc1ccccc1
2-amino-4-methylthiazole-5-carboxylic acid benzylamide
COc1cccc(C(=O)Nc2nc(C)c(C(=O)NCc3ccccc3)s2)c1
title compound
المردود 34.0%
COc1cccc(C(=O)Nc2nc(C)c(C(=O)NCc3ccccc3)s2)c1
2-(3-Methoxybenzoylamino)-4-methylthiazole-5-carboxylic Acid Benzylamide
المردود 34.0%

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

الإجراء التجريبي

Following the procedure as described in Example 2, making variations only as required to use 3-methoxybenzoyl chloride in place of benzoyl chloride to react with 2-amino-4-methylthiazole-5-carboxylic acid benzylamide, the title compound was obtained as a white solid in 34% yield; m.p. 75-77° C.; 1H NMR (CDCl3, 300 MHz) δ 7.43-7.31 (m, 8H), 7.12 (td, J=2.4, 6.7 Hz, 1H), 5.97 (t, J=5.6 Hz, 1H), 4.58 (d, J=5.6 Hz, 2H), 3.82 (s, 3H), 2.47 (s, 3H); MS (ES+) m/z 382.1 (M+1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08541457B2uspto-grants-2013_09