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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397190Generated: October 29, 2026

2-Aminothiazole → Rac-2-(3,4-dichloro-phenyl)-2-[(tetrahydro-pyran-4-yl)oxy]-n-thiazol-2-yl-acetamide

https://huagongshe.com/reaction/397190

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantRac-(3,4-dichloro-phenyl)-[(tetrahydro-pyran-4-yl)oxy]-acetic acidHCID 18172603—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductRac-2-(3,4-dichloro-phenyl)-2-[(tetrahydro-pyran-4-yl)oxy]-n-thiazol-2-yl-acetamideHCID 1027151986%

Reaction Conditions

Temperature25 °C

Reaction Steps

A solution of rac-(3,4-dichloro-phenyl)-[(tetrahydro-pyran-4-yl)oxy]-acetic acid (90 mg, 0.30 mmol) in dichloromethane (10 mL) was treated with BOP reagent (195 mg, 0.44 mmol), triethylamine (0.12 mL, 0.88 mmol), and 2-aminothiazole (44 mg, 0.44 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 residual material was purified by flash chromatography (Merck Silica gel 60, 230-400 mesh, 90/10 hexanes/ethyl acetate) to give rac-2-(3,4-dichloro-phenyl)-2-[(tetrahydro-pyran-4-yl)oxy]-N-thiazol-2-yl-acetamide (98 mg, 86% yield) as a white foam: EI-HRMS m/e calcd for C16H16Cl2O3N2S (M+) 386.0258, found 386.0261.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608218B2
Source datasetuspto-grants-2003_08
ORD IDord-66da57734e134280ab57c2b409ff3bc1
Source noteuspto-grants-2003_08