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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1421907Generated: October 30, 2026

4-(Chloromethyl)-1-trityl-1H-imidazole → 2-(Benzylidene-amino)-3-(1-trityl-1H-imidazol-4-yl)-2-(1-trityl-1H-imidazol-4-ylmethyl)-propionic acid methyl ester

https://huagongshe.com/reaction/1421907

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chloromethyl)-1-trityl-1H-imidazoleHCID 2763176—
ReactantPotassium bis(trimethylsilyl)amideHCID 3251421—
ReactantMethyl [(phenylmethylidene)amino]acetateHCID 4169153—
SolventTetrahydrofuranHCID 8028—
Product2-(Benzylidene-amino)-3-(1-trityl-1H-imidazol-4-yl)-2-(1-trityl-1H-imidazol-4-ylmethyl)-propionic acid methyl esterHCID 15491432—

Reaction Steps

A solution of potassium bis(trimethylsilyl)amide (11.34 g, 54 mmol) in THF (100 ml) was added dropwise to a mixture of (benzylidene-amino)-acetic acid methyl ester (3.83 g, 21.63 mmol) and 4-chloromethyl-1-trityl-1H-imidazole (21.6 g, 60.18 mmol) in THF (200 ml) at -78° C. The resulting solution was warmed to ambient temperature and stirred for 24 hours. After removal of THF, the reaction mixture was subsequently partitioned between ethyl acetate and brine. The aqueous layer was washed two times with ethyl acetate. The ethyl acetate extracts were combined, dried over MgSO4, filtered and concentrated to give the crude title compound of example 1A.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06080769
Source datasetuspto-grants-2000_06
ORD IDord-eba7804e539c4a9f956c42c77e70fe10
Source noteuspto-grants-2000_06