Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1383970Generated: November 2, 2026

Ammonium Hydroxide → 1-[3-(Carbamoyl)butyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazole

https://huagongshe.com/reaction/1383970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant1-[3-(Chlorocarbonyl)butyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazoleHCID 21188745—
SolventMethanolHCID 887—
Product1-[3-(Carbamoyl)butyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazoleHCID 2118858073%

Reaction Steps

In an ammonium hydroxide solution (28%, 10 ml) was placed 1-[3-(chlorocarbonyl)butyl]-2-[(4-chlorophenoxy)methyl]-4-methylbenzimidazole (400 mg, 1.0 mmol). To this mixture 10 ml of methanol were added, to enhance solubility and the mixture was stirred for about 64 hours at room temperature. The reaction mixture was then concentrated under reduced pressure to produce a tan foam. The crude material was further purified by flash silica gel chromatography, eluting with a gradient solvent of 19:1 ethyl acetate:methanol to 9:1 ethyl acetate:methanol. The fractions containing the desired material were combined and concentrated in vacuo to yield 300 mg (73%) of the desired title compound as a white foam.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06255494B1
Source datasetuspto-grants-2001_07
ORD IDord-90860ef74b6c4ef8b941c01bf9cf6dd0
Source noteuspto-grants-2001_07