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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1595402Generated: November 1, 2026

Acetoxyacetyl chloride → HCID 178476484, compound

https://huagongshe.com/reaction/1595402

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoxyacetyl chlorideHCID 26297—
ReactantHCID 178424019HCID 178424019—
SolventPyridineHCID 1049—
ProductHCID 178476484HCID 178476484—

Reaction Steps

2-(4-Aminophenyl)-5-(4-methylphenyl)-N-(2-thiazolyl)-imidazole-4-carboxamide (0.30 g) obtained in Example 21 was dissolved in pyridine (20 ml) and acetoxyacetyl chloride (0.1 ml) was added dropwise under ice-cooling. The mixture was stirred at room temperature for 4 hr. The reaction mixture was concentrated and the residue was purified by silica gel chromatography using, as a mobile phase, chloroform/ethyl acetate=20:1. Theresidue was recrystallized from ethyl acetate to give 4-[5-(4-methylphenyl)-4-(2-thiazolylcarbamoyl)imidazol-2-yl]phenylcarbamoylmethyl acetate (0.13 g), melting point 250° C. or above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06288061B1
Source datasetuspto-grants-2001_09
ORD IDord-ef9cd3cd73da433da1a6c47031c44b11
Source noteuspto-grants-2001_09