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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062670Generated: October 26, 2026

Methylthiourea → 2-(Methylamino)-4-(3-cyanophenyl)-5-carboethoxythiazole

https://huagongshe.com/reaction/1062670

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethylthioureaHCID 2723704—
ReactantEthyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionateHCID 22282470—
SolventTetrahydrofuranHCID 8028—
Product2-(Methylamino)-4-(3-cyanophenyl)-5-carboethoxythiazoleHCID 2228246373%

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of ethyl 2-bromo-3-(3-cyanophenyl)-3-oxopropionate (0.65 g, 2.2 mmol) in 20 mL of tetrahydrofuran was added N-methylthiourea (0.20 g, 2.2 mmol). The resulting mixture was stirred at 65° C. for 16 h. The reaction was allowed to cool and the solvent was evaporated in vacuo. The residue was taken up in ethyl acetate, washed with saturated aq NaHCO3 and brine, dried (MgSO4) and concentrated in vacuo to yield a solid. Trituration with hexanes/ethyl ether left the title compound as an off-white solid (0.46 g, 73%). MS (ESI) 288.3 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06962935B2
Source datasetuspto-grants-2005_11
ORD IDord-8d02aa7c04fe4e08bf4cbdbd2d5fb687
Source noteuspto-grants-2005_11