تفاعل #1265393

ord-1a8ebb4b788d47fd9d5effa2739075de

معادلة التفاعل

Cc1cc(C)cc(NC(N)=[NH2+])c1.O=[N+]([O-])[O-]
N-(3,5 dimethylphenyl) guanidinium nitrate
CC(=O)c1ncc(N(C)C)s1
1-(5-Dimethylamino-thiazol-2-yl)-ethanone
CNC
dimethylamine
CC(=O)c1ncc(Br)s1
1-(5-Bromo-thiazol-2-yl)-ethanone
Cc1cc(C)cc(Nc2nccc(-c3ncc(N(C)C)s3)n2)c1
[4-(5-Dimethylamino-thiazol-2-yl)-pyrimidin-2-yl]-(3,5-dimethyl-phenyl)-amine

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىprepared
  2. 2
    أخرىThe product was isolated as a yellow solid (40% last step)

الإجراء التجريبي

This compound was prepared from 1-(5-Dimethylamino-thiazol-2-yl)-ethanone (prepared from dimethylamine and 1-(5-Bromo-thiazol-2-yl)-ethanone in a procedure similar to that described in method I) and N-(3,5 dimethylphenyl) guanidinium nitrate (prepared using a procedure similar to that described in WO9719065) using procedures similar to those described in methods E-F. The product was isolated as a yellow solid (40% last step); IR (solid) 1738, 1365, 1217, cm−1; 1H NMR (400 Mhz, CDCl3) δ 2.35 (6H, s), 3.1 (6H, s), 6.75 (1H, s), 7.00 (1H, s), 7.37 (1H, s), 7.4 (2H, s), 8.45 (1H, d);); MS (ES+) 326.2 (M+1), (ES−) 324.2 (M−1).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07276502B2uspto-grants-2007_10