تفاعل #1521838

ord-0d3060dd743d4081b61e835cee2fed94

معادلة التفاعل

Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
N′-(2-thiazolyl)sulfanilamide
c1ccncc1
pyridine
ClCCl
DCM
CC(Cl)C(=O)Cl
2-chloro-propionylchloride
O=C(CCCl)Nc1ccc(S(=O)(=O)Nc2nccs2)cc1
3-Chloro-N-[4-(thiazol-2-ylsulfamoyl)-phenyl]-propionamide

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىSynthesized

الإجراء التجريبي

Synthesized according to general procedure 1: N′-(2-thiazolyl)sulfanilamide (8.37 g, 32.8 mmol), pyridine (5.3 mL, 65.6 mmol), 2-chloro-propionylchloride (3.8 mL, 39.4 mmol, 1.2 equiv) in DCM (400 mL). Yield: 2.70 g (24%) of a white solid. 1H-NMR (DMSO-d6) δ 10.41 (s, 1H), 7.77-7.72 (m, 4H), 7.25 (d, J=4.6 Hz, 1H), 6.82 (d, J=4.6 Hz, 1H), 3.88 (t, J=6.2 Hz, 2H), 2.86 (t, J=6.2 Hz, 2H). LC/MS (10-99%) M/Z: M+1 obs=346.1; tR=1.94 min.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07615563B2uspto-grants-2009_11