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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 444889Generated: October 29, 2026

Water → 4-Methyl-5-(2-(1,1,1-trifluoro-2-methylpropan-2-yl)pyrimidin-4-yl)thiazol-2-amine

https://huagongshe.com/reaction/444889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
ReactantN'-[5-((E)-3-dimethylamino-acryloyl)-4-methyl-thiazol-2-yl]-N,N-dimethylformamidineHCID 67218484—
ReactantHCID 86641156HCID 86641156—
Solvent2-MethoxyethanolHCID 8019—
Product4-Methyl-5-(2-(1,1,1-trifluoro-2-methylpropan-2-yl)pyrimidin-4-yl)thiazol-2-amineHCID 59293733—

Reaction Conditions

Temperature125 °C

Reaction Steps

Powdered sodium hydroxide (0.42 g) is added to a solution of N′-[5-((E)-3-dimethylamino-acryloyl)-4-methyl-thiazol-2-yl]-N,N-dimethyl-formamidine (0.93 g, prepared as described by S. Wang et al J. Med. Chem. 2004, 47, 1662-1675.) and 3,3,3-trifluoro-2,2-dimethyl-propionamidine hydrochloride (0.54 g) in 2-methoxyethanol (7 ml) and the mixture is heated at 125° C. for 1 hour with stirring. The reaction mixture is cooled, water is added, and the aqueous layer is extracted 4-times with 10% methanol in dichloromethane. The combined organic layers are purified by reversed phase chromatography and sodium bicarbonate is added to the fractions containing the title compound to give a white precipitate, which is collected by filtration. HPLC/MS: retention time 1.47 minutes, M+H 303.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476268B2
Source datasetuspto-grants-2013_07
ORD IDord-68d860bf1eff41409f84a6d10ffba62f
Source noteuspto-grants-2013_07