反应 #1797548

ord-51547afed8134322bacb0dde7e9ab27d

反应方程式

S=C1CCCCC(CCc2nc3cc(-c4ccccc4)cnc3[nH]2)N1
7-[2-(6-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-thione
S=C1CCCCC(CCc2nc3cc(-c4ccccc4)cnc3[nH]2)N1
compound A1
S=C1CCCCC(CCc2nc3cc(-c4ccccc4)cnc3[nH]2)N1
7-[2-(6-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-thione
N
ammonia
NC1=NC(CCc2nc3cc(-c4ccccc4)cnc3[nH]2)CCCC1
title compound
NC1=NC(CCc2nc3cc(-c4ccccc4)cnc3[nH]2)CCCC1
7-[2-(6-Phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-4,5,6,7-tetrahydro-3H-azepin-2-ylamine

溶剂

反应条件

温度
50°CELSIUS
详细条件
See reaction.notes.procedure_details.

后处理

  1. 1
    其他Subsequently, the reaction mixture is evaporated to dryness
  2. 2
    其他purified by flash chromatography on LiChroprep-NH2® (eluent gradient: dichloromethane/0-100 vol. % methanol)

实验过程

65 mg of 7-[2-(6-phenyl-3H-imidazo[4,5-b]pyridin-2-yl)-ethyl]-azepan-2-thione (compound A1) are suspended in 4.3 ml of methanol containing ammonia (strength: 7.0 M) and heated at 50° C. for 90 hours. Subsequently, the reaction mixture is evaporated to dryness and purified by flash chromatography on LiChroprep-NH2® (eluent gradient: dichloromethane/0-100 vol. % methanol), and lyophilized from 2.0 ml of water, 5.0 ml of dioxane to afford 29.5 mg of the title compound as an amorphous, colorless solid of m.p. 117° C. (decomp.). ESI-MS: 334.3 (MH+). TLC: Rf=0.35 (LiChroprep-NH2® HPTLC, methanol/water 10:1 parts by volume).

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07790710B2uspto-grants-2010_09