反应 #1702108
ord-2549c43191ae45c5a2bbda11ef5e715e
反应方程式
反应物
溶剂
反应条件
后处理
- 1其他the resulting mixture was degassed with nitrogen for an additional 5 minutes after which the reaction
- 2其他was placed in a 80° C.
- 3温度heated for 3.5 h
- 4温度The reaction was cooled
- 5其他partitioned between ethyl acetate and sat. NaHCO3
- 6其他The organic layer was separated
- 7洗涤washed with 5% LiCl, brine
- 8干燥dried over Na2SO4
- 9浓缩concentrated
- 10其他to give a dark brown foam
- 11其他Purification by flash column chromatography on silica gel using 30% ethyl acetate in hexanes
实验过程
A solution of 3,3-dimethyl-pent-4-yn-1-ol (600 mg, 5.36 mmol), 3-[[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester (2767 mg, 4.46 mmol) and triethylamine (10.8 mL, 77.48 mmol) in DMF (25 mL) was degassed for 10 minutes with nitrogen. PdCl2(PPh3)2 (314 mg, 0.45 mmol) and CuI (170 mg, 0.90 mmol) was added and the resulting mixture was degassed with nitrogen for an additional 5 minutes after which the reaction was placed in a 80° C. oil bath and heated for 3.5 h. The reaction was cooled and partitioned between ethyl acetate and sat. NaHCO3. The organic layer was separated, washed with 5% LiCl, brine, dried over Na2SO4 and concentrated to give a dark brown foam. Purification by flash column chromatography on silica gel using 30% ethyl acetate in hexanes then 5% methanol in ethyl acetate provided 3-[[4-(tert-butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-(5-hydroxy-3,3-dimethyl-pent-1-ynyl)-thiophene-2-carboxylic acid methyl ester (2.43 g, 90%) as a pale yellow foam.