반응 #41168
ord-b0eb15d1b2804e658d0348c324e84c96
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용매
반응 조건
후처리
- 1온도cooled slightly
- 2온도After cooling to room temperature
- 3기타the mixture was partitioned between methylene chloride and water
- 4세척The aqueous phase was washed with a second portion of methylene chloride
- 5세척washed with brine
- 6건조dried over sodium sulfate
- 7농축concentrated
- 8세척Flash chromatography, eluting with a 0-20% methanol/ethyl acetate gradient
- 9기타separated
- 10workup.ADDITIONa large portion of the cis-trans mixture of isomers
- 11기타crystallized from EtOAc-hexanes
실험 절차
Hydrazino-cyclohexanol hydrochloride (1.920 g, 9.79 mmol) was dissolved in hot ethanol and then cooled slightly. Ethyl (ethoxymethylene)-cyanoacetate (1.520 g, 8.98 mmol) and anhydrous sodium acetate (2.013 g, 24.54 mmol) were added and the mixture was heated at 70° C. for 15 hours. After cooling to room temperature, the mixture was partitioned between methylene chloride and water. The aqueous phase was washed with a second portion of methylene chloride. The two organic phases were combined, washed with brine, dried over sodium sulfate and concentrated. Flash chromatography, eluting with a 0-20% methanol/ethyl acetate gradient, separated a large portion of the cis-trans mixture of isomers. After chromatography, pure fractions of each isomer were combined and crystallized from EtOAc-hexanes to give 5-amino-1-(cis-4-hydroxy-cyclohexyl)-1H-pyrazole-4-carboxylic acid ethyl ester (0.511 g, 23% (crop 1); 0.121 g, 5% (crop 2)) and 5-amino-1-(trans-4-hydroxy-cyclohexyl)-1H-pyrazole-4-carboxylic acid ethyl ester (0.625 g, 28%).