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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516240Generated: November 4, 2026

Methyl iodide → 4-Methyl-5-(2-(methylthio)pyrimidin-4-yl)thiazol-2-amine

https://huagongshe.com/reaction/1516240

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantSodium HydroxideHCID 14798—
ReactantThioureaHCID 2723790—
ReactantN'-[5-(3-dimethylamino-acryloyl)-4-methyl-thiazol-2-yl]-N,N-dimethyl-formamidineHCID 67218485—
SolventEthanolHCID 702—
SolventWaterHCID 962—
Product4-Methyl-5-(2-(methylthio)pyrimidin-4-yl)thiazol-2-amineHCID 57506656—

Reaction Steps

Powdered sodium hydroxide (1.09 g) is added to a solution of N′-[5-(3-dimethylamino-acryloyl)-4-methyl-thiazol-2-yl]-N,N-dimethyl-formamidine (2.0 g, prepared as described by S. Wang et al J. Med. Chem. 2004, 47, 1662-1675.) and thiourea (0.57 g) in ethanol (25 ml) and the mixture is heated at reflux for 3 hour with stirring. The reaction mixture is cooled to room temperature and water then methyliodide (0.47 ml) is added. After 1 hour at room temperature the ethanol is removed by evaporation and water is added and the pH is adjusted to 7 with 2N aqueous hydrochloric acid. The title compound is then obtained by filtration. ESI-MS: M+H 239 and M−H 237.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227462B2
Source datasetuspto-grants-2012_07
ORD IDord-5c80559595c8480b92590457c2900ed3
Source noteuspto-grants-2012_07