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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1936270Generated: November 1, 2026

2-Aminothiazole → HCID 10222775, compound

https://huagongshe.com/reaction/1936270

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
ReactantTriethylamineHCID 8471—
ReactantBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
ReactantHCID 67484028HCID 67484028—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 10222775HCID 1022277554%

Reaction Steps

A solution of 3-cyclopentyl-2-(4-pyrimidin-5-ylethynyl-phenyl)-propionic acid (150 mg, 0.53 mmol), benzotriazol-1-yloxytris(dimethylamino)phosphonium hexafluorophosphate (376 mg, 0.85 mmol), triethylamine (0.22 mL, 1.59 mmol) and 2-aminothiazole (85 mg, 0.85 mmol) in methylene chloride (5 mL) was stirred at 25° C. for 18 h. At this time, the reaction was diluted with water (10 mL). The organic phase was separated and washed with a 1N aqueous sodium hydroxide solution, and a saturated aqueous sodium chloride solution. The aqueous layers were each back-extracted with methylene chloride. The combined organic extracts were dried over magnesium sulfate, filtered, and concentrated in vacuo. Flash chromatography (Merck Silica gel 60, 230-400 mesh, 60/40 hexanes/ethyl acetate) afforded 3-cyclopentyl-2-(4-pyrimidin-5-ylethynyl-phenyl)-N-thiazol-2-yl-propionamide (102 mg, 54%) as a white solid: mp 149-151 ° C.; EI-HRMS m/e calcd for C23H22N4OS (M+) 402.1514, found 402.1516.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06388071B2
Source datasetuspto-grants-2002_05
ORD IDord-d38f40503cdb4a08aa78c635f7ed0a69
Source noteuspto-grants-2002_05