Реакция #640533

ord-8b9f34435be842cf8a5fb4b6184f2648

Уравнение реакции

COc1cc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)ccc1O
4-[1-(3-methoxy-4-hydroxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine
CCN(C(C)C)C(C)C
DIPEA
COCCl
methoxymethyl chloride
COCOc1ccc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)cc1OC
title compound
COCOc1ccc(C(=O)Cn2c(-c3nonc3N)nc3ccccc32)cc1OC
4-[1-(3-Methoxy-4-methoxymethoxy-phenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with water
  2. 2
    Сушкаdried over sodium sulphate
  3. 3
    ФильтрацияFiltration of the sodium sulphate and concentration of the filtrate under reduced pressure

Методика

A mixture of 4-[1-(3-methoxy-4-hydroxyphenacyl)-1H-benzimidazol-2-yl]-furazan-3-ylamine (0.10 g, 0.27 mmol), DIPEA and methoxymethyl chloride in dry DMF is stirred at room temperature for 14 hours. The reaction mixture is diluted with ethyl acetate, washed with water and dried over sodium sulphate. Filtration of the sodium sulphate and concentration of the filtrate under reduced pressure gives the title compound as colorless, pure solid, m.p. 190° C.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE042890E1uspto-grants-2011_11