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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2072723Generated: November 1, 2026

Benzoyl chloride → 2-Benzamido-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole

https://huagongshe.com/reaction/2072723

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl chlorideHCID 7412—
ReactantTriethylamineHCID 8471—
Reactant2-Amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazoleHCID 10469982—
SolventTetrahydrofuranHCID 8028—
Product2-Benzamido-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazoleHCID 1567604269%

Reaction Steps

To 2-amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole (300 mg, 1.01 mmol) in tetrahydrofuran (15 ml) was added benzoyl chloride (145 mg, 1.03 mmol) and triethylamine (101 mg, 1.00 mmol) and the mixture was stirred at room temperature overnight. After reaction, the reaction mixture was filterated and evaporated under reduced pressure to a residue, which was chromatographed to afford 2-benzamido-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole (279 mg, 69% yield): mp 147°-147.5° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04914112
Source datasetuspto-grants-1990_04
ORD IDord-cd03eb8e78064ef3b9075e7073ad1dd1
Source noteuspto-grants-1990_04