tert-butyl 5-(N'-methyl-N'-phenylhydrazinocarbonyl)-3-(3-morpholin-4-ylmethylbenzoylamino)thieno[2,3-c]pyrazole-1-carboxylate 、
tert-butyl 5-(N'-(4-chlorophenyl)-N'-methylhydrazinocarbonyl)-3-(3-morpholin-4-ylmethylbenzoylamino)thieno[2,3-c]pyrazole-1-carboxylate 以
甲醇 为溶剂,
40.0~100.0 ℃
、266.64 kPa
条件下,
反应 0.5h,
以105 mg of N-[5-(N′-methyl-N′-phenylhydrazinocarbonyl)-1H-thieno[2,3-c]pyrazol-3-yl]-3-morpholin-4-ylmethylbenzamide are thus obtained in the form of a yellow powder的产率得到N-[5-(N'-methyl-N'-phenylhydrazinocarbonyl)-1H-thieno[2,3-c]pyrazol-3-yl]-3-morpholin-4-ylmethylbenzamide