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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 430287Generated: October 30, 2026

2-Aminothiazole → HCID 22315154, compound

https://huagongshe.com/reaction/430287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTriphenylphosphineHCID 11776—
ReactantN-bromobutanimideHCID 67184—
ReactantHCID 22315251HCID 22315251—
SolventDichloromethaneHCID 6344—
ProductHCID 22315154HCID 2231515462%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of triphenylphosphine (154 mg, 0.59 mmol) in methylene chloride (2 mL) was cooled to 0° C. and then slowly treated with N-bromosuccinimide (105 mg, 0.59 mmol). The reaction mixture was stirred at 0° C. for 10 min and then treated with 2-(3,4-bis-methanesulfonyl-phenyl)-3-cyclopentyl-propionic acid (200 mg, 0.53 mmol). The resulting reaction mixture was stirred at 0° C. for 5 min and then allowed to warm to 25° C. where it was stirred for 30 min. The reaction mixture was then treated with 2-aminothiazole (118 mg, 1.18 mmol). The resulting reaction mixture was stirred at 25° C. for 15 h. The crude reaction mixture was then directly purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 1/1 hexanes/ethyl acetate) to afford 2-(3,4-bis-methanesulfonyl-phenyl)-3-cyclopentyl-N-thiazol-2-yl-propionamide (150 mg, 61%) as a pale yellow foam: mp 104-107° C.; EI-HRMS m/e calcd for C19H24N2O5S3 (M+) 456.0847, found 456.0846.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06320050B1
Source datasetuspto-grants-2001_11
ORD IDord-ecac73c0aa224ea4bc8788cb67fadbc9
Source noteuspto-grants-2001_11