反应 #636232

ord-8dcf39505b974879aeca7eda79ac228d

反应方程式

COCC(C)O
1-methoxy-2-propanol
c1ccc(P(c2ccccc2)c2ccccc2)cc1
triphenylphosphine
CC(C)OC(=O)[N+](=[N-])C(=O)OC(C)C
diisopropyldiazodicarboxylate
Cc1ccc(S(=O)(=O)n2c(-c3cn(C)c4ccc(O)cc34)cc3cccnc32)cc1
1-methyl-3-[1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-1H-indol-5-ol
COCC(C)Oc1ccc2c(c1)c(-c1cc3cccnc3n1S(=O)(=O)c1ccc(C)cc1)cn2C
title compound
COCC(C)Oc1ccc2c(c1)c(-c1cc3cccnc3n1S(=O)(=O)c1ccc(C)cc1)cn2C
2-[5-(2-Methoxy-1-methyl-ethoxy)-1-methyl-1H-indol-3-yl]-1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridine

溶剂

反应条件

详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    温度The resulting mixture was heated
  2. 2
    温度under reflux for 5 hours
  3. 3
    温度then cooled
  4. 4
    其他evaporated
  5. 5
    workup.ADDITIONThe residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:1

实验过程

A solution of triphenylphosphine (470 mg) and diisopropyldiazodicarboxylate (350 μl) in dry toluene (15 mL) was treated with 1-methyl-3-[1-(toluene-4-sulfonyl)-1H-pyrrolo[2,3-b]pyridin-2-yl]-1H-indol-5-ol [150 mg, Reference Example 14(a)] followed by 1-methoxy-2-propanol (150 μl). The resulting mixture was heated under reflux for 5 hours then cooled and then evaporated. The residue was subjected to flash chromatography on silica eluting with a mixture of ethyl acetate and pentane (1:1, v/v) to give the title compound (50 mg) as a clear oil. TLC: RF=0.65 (pentane/ethyl acetate: 1/1). MS: 480 (MH+).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07943616B2uspto-grants-2011_05