反应 #1702162

反应方程式

tert-butyl (5-ethynylpyridin-3-yl)carbamate

tert-Butyl (5-ethynylpyridin-3-yl)carbamate

tert-butyl (4-cyano-2-iodophenyl)carbamate

triethylamine

→

desired product

收率 52.8%

tert-Butyl [5-({2-[(tert-butoxycarbonyl)amino]-5-cyanophenyl}ethynyl)pyridin-3-yl]carbamate

收率 52.8%

溶剂

tetrahydrofuran

反应条件

后处理

1. 1
   workup.STIRRINGThe reaction mixture was stirred at 65° C. for 2 hours
2. 2
   其他The solvent was removed under vacuum
3. 3
   workup.ADDITIONthe residue was diluted with EtOAc and water
4. 4
   其他After separation
5. 5
   干燥the organic layer was dried over Na2SO4
6. 6
   浓缩concentrated under vacuum
7. 7
   其他The crude was purified by silica gel column chromatography

实验过程

Into a reaction flask were added tert-butyl (4-cyano-2-iodophenyl)carbamate (1.4 g, 4.1 mmol), copper(I) iodide (31 mg, 0.16 mmol), bis(triphenylphosphine)palladium(II) chloride (0.12 g, 0.16 mmol), tetrahydrofuran (10 mL), and triethylamine (0.63 mL, 4.5 mmol). The mixture was stirred under N2 bubbling for 5 minutes and tert-butyl (5-ethynylpyridin-3-yl)carbamate (0.90 g, 4.1 mmol) (prepared according to Example 17, Step B) was then added. The reaction mixture was stirred at 65° C. for 2 hours. The solvent was removed under vacuum and the residue was diluted with EtOAc and water. After separation, the organic layer was dried over Na2SO4 and concentrated under vacuum. The crude was purified by silica gel column chromatography to give the desired product (0.94 g, 52%). LCMS for C24H27N4O4 (M+H)+: m/z=435.2.

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