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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 6484Generated: October 28, 2026

2-n-butyl 4-chloro 1-(2-chlorophenyl)methyl-5-hydroxymethyl-1H-imidazole → {1-(2-chlorophenyl)methyl-2-n butyl-1H-imidazol-5-yl}methyl-alpha-ethylphenylalanine methyl ester

https://huagongshe.com/reaction/6484

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-n-butyl 4-chloro 1-(2-chlorophenyl)methyl-5-hydroxymethyl-1H-imidazoleHCID 13074095—
Reactanta-Ethylphenylalanine methyl esterHCID 53840745—
Product{1-(2-chlorophenyl)methyl-2-n butyl-1H-imidazol-5-yl}methyl-alpha-ethylphenylalanine methyl esterHCID 53794162—

Reaction Steps

The procedure of Example 4 (i), Method A, was followed using a-ethylphenylalanine methyl ester in place of α-methyl-phenylalanine methyl ester to give N-[{1-(2-chlorophenyl)methyl-2-n butyl-1H-imidazol-5-yl}methyl-α-ethylphenylalanine methyl ester. Hydrolysis of the ester using the procedure of Example 2 (ii), followed by treatment with hydrochloric acid, gave the title compound as the dihydrochloride salt; mp 209°-211° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05248689
Source datasetuspto-grants-1993_09
ORD IDord-36b3c2ed1dbc482aa4b7a196ab5747d7
Source noteuspto-grants-1993_09