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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 433574Generated: October 29, 2026

Ethyl Acetate → HCID 69041919, compound

https://huagongshe.com/reaction/433574

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69040616HCID 69040616—
SolventEthyl orthoformateHCID 31214—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 69041919HCID 69041919—

Reaction Steps

A suspension of 1-[1-(3,4-dichloro-phenyl)-1H-imidazol-4-ylmethyl]-1H-imidazol-2-ylamine (0.7 g, 2.3 mmol) in triethyl orthoformate (10 ml) was stirred under reflux for 2 h. The reaction mixture was evaporated to dryness, dissolved in ethanol (10 ml) and cooled in an ice bath. Sodium borohydride (0.091 g, 2.4 mmol) was added and the mixture was allowed to slowly reach 20° C. After 18 h AcOEt and brine was added and the organic phase was separated, dried (Na2SO4) and concentrated. After chromatography [silica, elution with gradient CH2Cl2 to 100% (CH2Cl2/MeOH/aq. NH4OH=90:10:1)] the free base of the title compound was obtained. It was crystallized as the off-white hydrochloride salt (0.25 g; 16%). Mp. >250° C. (MeOH/Et2O), MS: m/e=322 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06667335B2
Source datasetuspto-grants-2003_12
ORD IDord-af40f3f0dda44c8bb69ffe21e1dbf6ad
Source noteuspto-grants-2003_12