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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646562Generated: November 2, 2026

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

https://huagongshe.com/reaction/1646562

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, 1.101 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 cromatographed 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 numberUS05180731
Source datasetuspto-grants-1993_01
ORD IDord-d503174608f44197aaefea7d8fede616
Source noteuspto-grants-1993_01