تفاعل #691644

ord-f4c67bcde69443aa9b5349e312d323ce

معادلة التفاعل

COc1ccc(-c2nc(COc3ccc(S(=O)(=O)Cl)cc3)co2)cc1
4-[2-(4-Methoxy-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonyl chloride
CC(C)c1nnc(N)s1
5-isopropyl-[1,3,4]thiadiazol-2-ylamine
COc1ccc(-c2nc(COc3ccc(S(=O)(=O)Nc4nnc(C(C)C)s4)cc3)co2)cc1
N-(5-Isopropyl-[1,3,4]thiadiazol-2-yl)-4-[2-(4-methoxy-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonamide
المردود 2.6%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe pyridine was removed in vacuo
  2. 2
    أخرىThe residue was purified by RP-HPLC

الإجراء التجريبي

580 mg 4-[2-(4-Methoxy-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonyl chloride were added to a stirred solution of 275 mg 5-isopropyl-[1,3,4]thiadiazol-2-ylamine in 35 ml pyridine. 18 mg 4-Dimethylaminopyridine were added. The reaction mixture was stirred at room temperature overnight. The pyridine was removed in vacuo and the residue coevaporated with 15 ml toluene. The residue was purified by RP-HPLC to obtain 19 mg N-(5-Isopropyl-[1,3,4]thiadiazol-2-yl)-4-[2-(4-methoxy-phenyl)-oxazol-4-ylmethoxy]-benzenesulfonamide.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07910612B2uspto-grants-2011_03