反应 #684975

ord-8329962600884965a21ddaff632a83b7

反应方程式

CCOC(C)=O
ethyl acetate
O=C([O-])[O-].[K+].[K+]
Potassium carbonate
CI
methyl iodide
Oc1cccnc1Cc1ccc(Br)cc1F
compound
Oc1cccnc1Cc1ccc(Br)cc1F
2-(4-Bromo-2-fluorobenzyl)-3-pyridinol
COc1cccnc1Cc1ccc(Br)cc1F
title compound
收率 84.4%
COc1cccnc1Cc1ccc(Br)cc1F
2-(4-Bromo-2-fluorobenzyl)-3-methoxypyridine
收率 84.4%

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    洗涤the reaction mixture was washed with saturated brine
  2. 2
    浓缩concentrated under reduced pressure
  3. 3
    其他The residue was purified by silica gel column chromatography

实验过程

Potassium carbonate (38.7 mg, 0.280 mmol) and methyl iodide (10.5 μl, 0.168 mmol) were added to a solution of the compound of Example B245 (15.8 mg, 0.0560 mmol) in dimethylformamide (1 ml), and this reaction mixture was stirred at room temperature for 2 hours. After ethyl acetate was added, the reaction mixture was washed with saturated brine and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give the title compound (14.0 mg).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07897387B2uspto-grants-2011_03