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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388914Generated: November 1, 2026

2-(4-(2,3-Epoxypropoxy)phenyl)acetamide → N-{3-[4-(2-amino-2-oxoethyl)phenoxy]-2-hydroxypropyl}-alpha-methyl-1H-benzimidazole-1-propanamine

https://huagongshe.com/reaction/1388914

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(2,3-Epoxypropoxy)phenyl)acetamideHCID 119857—
Reactant4-(1H-Benzo[d]imidazol-1-yl)butan-2-amineHCID 13267879—
SolventMethanolHCID 887—
ProductN-{3-[4-(2-amino-2-oxoethyl)phenoxy]-2-hydroxypropyl}-alpha-methyl-1H-benzimidazole-1-propanamineHCID 13066759—

Reaction Steps

A mixture of 1.65 grams of α-methyl-1H-benzimidazole-1-propanamine and 1.82 grams of 1-[4-(2-amino-2-oxoethyl)phenoxy]-2,3-epoxypropane in 6 ml. of 95 percent methanol was refluxed for 19 hours. The solvent was evaporated from the mixture and the residual solid was triturated several times with ether. The solid was then dried and chromatographed on a silica gel column using methanol. The fractions containing the desired product were determined by thin-layer chromatography and combined. The solvent was then evaporated to leave a residual oil which solidified on cooling to give N-{3-[4-(2-amino-2-oxoethyl)phenoxy]-2-hydroxypropyl}-α-methyl-1H-benzimidazole-1-propanamine melting at about 139°-142° C. This compound has the following structural formula. ##STR18##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04434174
Source datasetuspto-grants-1984_02
ORD IDord-2a512def4f07427bb14d02d63853ed0f
Source noteuspto-grants-1984_02