反应 #1447084

ord-d94e516bfa604dce9c64081db90e7423

反应方程式

C=CC(O)C(NC(=O)c1cn(C)nc1C(F)(F)F)C(=O)NC
N-(2-hydroxy-1-methylcarbamoylbut-3-enyl)-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxamide
CC(=O)O
acetic acid
CN(C)c1ccccn1
dimethylaminopyridine
C=CC(OC(C)=O)C(NC(=O)c1cn(C)nc1C(F)(F)F)C(=O)NC
1-{Methylcarbamoyl-[(1-methyl-3-trifluoromethyl-1H-pyrazole-4-carbonyl)amino]-methyl}allyl acetate

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤the reaction solution was washed
  2. 2
    其他the solvent was removed

实验过程

134 mg (0.42 mmol) of N-(2-hydroxy-1-methylcarbamoylbut-3-enyl)-1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxamide, 28 mg (0.46 mmol) of acetic acid and 20 mg (0.17 mmol) of dimethylaminopyridine were dissolved in CH2Cl2. At 0° C., 88 mg (0.46 mmol) of 1-(3-dimethylaminopropyl)-3-(ethylcarbodiimide) hydrochloride were added. After 16 h of stirring at RT, the reaction solution was washed and the solvent was removed. This gave 0.10 g (66% of theory) of the title compound as a colorless powder (M+(m/z)=362).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07879761B2uspto-grants-2011_02