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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397185Generated: October 29, 2026

2-Aminothiazole → Rac-2-cyclohexyloxy-2-(3,4-dichloro-phenyl)-n-thiazol-2-yl-acetamide

https://huagongshe.com/reaction/397185

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTriethylamineHCID 8471—
ReactantRac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acidHCID 12044175—
ReactantBenzotriazol-1-yloxy-(dimethylamino)phosphonium hexafluorophosphateHCID 131723656—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductRac-2-cyclohexyloxy-2-(3,4-dichloro-phenyl)-n-thiazol-2-yl-acetamideHCID 1017811488%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of rac-cyclohexyloxy-(3,4-dichloro-phenyl)-acetic acid (102 mg, 0.34 mmol) in dichloromethane (10 mL) was treated with benzotriazol-1-yloxy-(dimethylamino)phosphonium hexafluorophosphate (BOP) reagent (223 mg, 0.51 mmol), triethylamine (0.14 mL, 0.52 mmol), and 2-aminothiazole (51 mg, 0.51 mmol) at 25° C. After the resulting brownish-orange solution was stirred 16 h at 25° C., it was diluted with water (10 mL) and extracted with ethyl acetate (3×15 mL). The combined organic layers were washed with water (1×10 mL), 1N sodium hydroxide solution (1×10 mL), 1N hydrochloric acid (1×10 mL), and brine (1×10 mL), then were dried over sodium sulfate and evaporated in vacuo. The product was purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 90/10 hexanes/ethyl acetate) to furnish rac-2-cyclohexyloxy-2-(3,4-dichloro-phenyl)-N-thiazol-2-yl-acetamide (115 mg, 88% yield) as a white foam: EI-HRMS m/e calcd for C17H18Cl2O2N2S (M+) 384.0466, found 384.0469.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608218B2
Source datasetuspto-grants-2003_08
ORD IDord-230d953286d146829c736013adc6a8db
Source noteuspto-grants-2003_08