تفاعل #73611

ord-cf05cbdf891b4243bb4d432034c7cf46

معادلة التفاعل

O=C(Cl)C1CCCC1
cyclopentanecarbonyl chloride
Cc1nc(N)sc1C(=O)NCc1ccccc1
2-amino-4-methylthiazole-5-carboxylic acid benzylamide
Cc1nc(NC(=O)C2CCCC2)sc1C(=O)NCc1ccccc1
title compound
المردود 38.0%
Cc1nc(NC(=O)C2CCCC2)sc1C(=O)NCc1ccccc1
2-(Cyclopentanecarbonylamino)-4-methylthiazole-5-carboxylic Acid Benzylamide
المردود 38.0%

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 cyclopentanecarbonyl 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 38% yield; 1H NMR (CDCl3, 300 MHz) δ 9.56 (s, br, 1H), 7.35-7.24 (m, 5H), 5.92 (s, br, 1H), 4.56 (d, J=5.7 Hz, 2H), 2.81-2.69 (m, 1H), 2.62 (s, 3H), 1.97-1.72 (m, 8H); MS (ES+) m/z 344.2 (M+1).

المصدر

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