反应 #1005965

ord-1c9300ef120e4780b33c33be3ac91b33

反应方程式

FC(F)(F)c1ccc2nc(Br)cn2c1
2-bromo-6-trifluoromethyl-imidazo[1,2-a]pyridine
CCSc1ccccc1B1OC(C)(C)C(C)(C)O1
2-ethylsulfanylphenylboronic acid pinacol ester
C1CCC(P(C2CCCCC2)C2CCCCC2)CC1
tricyclohexylphosphine
O=P([O-])([O-])[O-].[K+].[K+].[K+]
tripotassium phosphate
CCSc1ccccc1-c1cn2cc(C(F)(F)F)ccc2n1
2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine
收率 89.1%

反应条件

温度
100°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    过滤the mixture was filtered
  2. 2
    萃取The aqueous layer of the filtrate was extracted with ethyl acetate
  3. 3
    洗涤the mixture was washed with water
  4. 4
    干燥dried over anhydrous magnesium sulfate
  5. 5
    浓缩The mixture was concentrated under reduced pressure

实验过程

A mixture of 526 mg of 2-bromo-6-trifluoromethyl-imidazo[1,2-a]pyridine, 576 mg of 2-ethylsulfanylphenylboronic acid pinacol ester, 50 mg of tris(dibenzylideneacetone) dipalladium(0), 201 mg of tricyclohexylphosphine (18% toluene solution), 1.26 g of tripotassium phosphate, 4.5 ml of 1,4-dioxane and 1.5 ml of water was stirred at 100° C. for 2.5 hours. Ethyl acetate and water were poured to the cooled reaction mixture, and the mixture was filtered. The aqueous layer of the filtrate was extracted with ethyl acetate, then combined with the organic layer of the filtrate, and the mixture was washed with water and dried over anhydrous magnesium sulfate. The mixture was concentrated under reduced pressure, and the resulting residue was applied to a silica gel column chromatography to obtain 570 mg of 2-(2-ethylsulfanylphenyl)-6-trifluoromethyl-imidazo[1,2-a]pyridine (hereinafter, referred to as Compound of Present Invention 4).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US09271500B2uspto-grants-2016_03