反应 #1104

ord-77b579259b0e47c2ac2dc691717deb93

反应方程式

Cl
HCl
COc1c(NC2CCC(=O)CC2)ccnc1C
4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine
C1CCOC1
THF
[Mg]
magnesium
CC(C)(C)c1ccc(CBr)cc1
4-tert-butylbenzyl bromide
COc1c(N(CC2=CCC(O)(C(C)(C)C)C=C2)C2CCCCC2)ccnc1C
4-(4-Hydroxy-4-tert-butylbenzylcyclohexylamino)-3-methoxy-2-methylpyridine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    萃取the mixture is extracted several times with ethyl acetate
  2. 2
    洗涤the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution
  3. 3
    其他Purification
  4. 4
    温度increasing amounts of methanol
  5. 5
    workup.ADDITIONare added

实验过程

A Grignard solution is prepared from 1.2 g of magnesium and 12.9 g of 90% strength 4-tert-butylbenzyl bromide in 100 ml of abs. ether. 2.9 g of 4-(4-oxocyclohexylamino)-3-methoxy-2-methylpyridine in 50 ml of absolute THF are added dropwise to this solution. After 17 hours at room temperature it is acidified with 25 ml of 2N HCl, the mixture is extracted several times with ethyl acetate and the combined ethyl acetate phases are washed with sodium hydrogen carbonate solution. Purification is carried out by column chromatography on silica gel using ethyl acetate to which increasing amounts of methanol are added.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US05723450uspto-grants-1998_03