反应 #1702108

ord-2549c43191ae45c5a2bbda11ef5e715e

反应方程式

C#CC(C)(C)CCO
3,3-dimethyl-pent-4-yn-1-ol
COC(=O)c1sc(I)cc1N(C(=O)C1CCC(C)CC1)C1CCC(O[Si](C)(C)C(C)(C)C)CC1
3-[[4-(tert-Butyl-dimethyl-silanyloxy)-cyclohexyl]-(4-methyl-cyclohexanecarbonyl)-amino]-5-iodo-thiophene-2-carboxylic acid methyl ester
CCN(CC)CC
triethylamine
COC(=O)c1sc(C#CC(C)(C)CCO)cc1N(C(=O)C1CCC(C)CC1)C1CCC(O[Si](C)(C)C(C)(C)C)CC1
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
收率 90.2%

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他the resulting mixture was degassed with nitrogen for an additional 5 minutes after which the reaction
  2. 2
    其他was placed in a 80° C.
  3. 3
    温度heated for 3.5 h
  4. 4
    温度The reaction was cooled
  5. 5
    其他partitioned between ethyl acetate and sat. NaHCO3
  6. 6
    其他The organic layer was separated
  7. 7
    洗涤washed with 5% LiCl, brine
  8. 8
    干燥dried over Na2SO4
  9. 9
    浓缩concentrated
  10. 10
    其他to give a dark brown foam
  11. 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.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US08765722B2uspto-grants-2014_07