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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1646564Generated: November 3, 2026

Triethylamine → 2-Methanesulfonylamino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole

https://huagongshe.com/reaction/1646564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2-Amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazoleHCID 10469982—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product2-Methanesulfonylamino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazoleHCID 1567604971%

Reaction Steps

To a mixture of 2-amino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole (500 mg, 1.68 mmol) and triethylamine (340 mg, 3.36 mmol) in tetrahydrofuran was added methanesulfonyl chloride (385 mg, 3.36 mmol) by portion and the mixture was stirred at room temperature overnight. The reaction mixture was diluted with water, extracted with ethyl acetate and evaporated under reduced pressure to a residue, which was chromatographed and then recrystallized to afford 2-methanesulfonylamino-4-(1-(2-fluoro-4-biphenylyl)ethyl)thiazole (447 mg, 71% yield): mp 127.5°-129.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05180731
Source datasetuspto-grants-1993_01
ORD IDord-db0df7dbe63f48b29caed240548bfc23
Source noteuspto-grants-1993_01