反応 #91979

ord-a5d7666c985140f4ac8bf14a7c3e8b1a

反応方程式

CC(C)CCON=O
isoamyl nitrite
ICI
Diiodomethane
CCOCc1nc(C#N)c(N)n1CC(C)(C)O
5-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile
CCOCc1nc(C#N)c(I)n1CC(C)(C)O
title compound
収率 57.3%
CCOCc1nc(C#N)c(I)n1CC(C)(C)O
2-(Ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-5-iodo-1H-imidazole-4-carbonitrile
収率 57.3%

反応条件

温度
80°CELSIUS
詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    温度After cooling to room temperature the mixture
  2. 2
    濃縮was concentrated in vacuo
  3. 3
    その他purified by flash chromatography (silica gel, 20% to 50% ethyl acetate in heptane)

実験手順

Diiodomethane (14.5 ml, 180 mmol) was added under argon with stirring to a suspension of 5-amino-2-(ethoxymethyl)-1-(2-hydroxy-2-methylpropyl)-1H-imidazole-4-carbonitrile (4.36 g, 18.3 mmol) in chloroform (170 mL). The reaction mixture was heated to 80° C., a solution of isoamyl nitrite (9.86 ml, 73.2 mmol) in chloroform (30 mL) was added with a syringe pump over a period of 40 min and the mixture was stirred for another 30 min at 80° C. After cooling to room temperature the mixture was concentrated in vacuo and purified by flash chromatography (silica gel, 20% to 50% ethyl acetate in heptane) to give the title compound (3.66 g, 57%) as brown oil; LC-MS (UV peak area, ESI) 90%, 350.0374 (MH+).

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09447097B2uspto-grants-2016_09