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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 224495Generated: October 30, 2026

Thiourea → 2-amino-4-[N-4-chlorophenyl-N-methyl(carbamoylmethyl)] thiazole

https://huagongshe.com/reaction/224495

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThioureaHCID 2723790—
Reactant4-bromo-4'-chloro-N-methylacetoacetanilideHCID 20297528—
SolventEthanolHCID 702—
Product2-amino-4-[N-4-chlorophenyl-N-methyl(carbamoylmethyl)] thiazoleHCID 5448471766.7%

Reaction Steps

A 500 ml reaction flask equipped with a condenser, magnetic stirrer, thermometer and heating mantle was charged with 20.2 g (0.066 mole) of 4-bromo-4'-chloro-N-methylacetoacetanilide, 200 ml of ethanol and 5.4 g (0.071 mole) of thiourea. The reaction solution was refluxed for three hours. After cooling, about one-half of the solvent was removed on the rotary evaporator and the solution was poured into 300 ml of water. After adding sufficient ammonium hydroxide to pH 8, additional water was added. The precipitated crystalline product was dried in a vacuum oven. There was obtained 12.4 g (66.7%) of white material, M.P. 148°-50°. N.M.R. (dimethyl-d6 sulfoxide, CDCl3) ∂3.2 (NCH3), 3.3 (CH2), 6.0 (heteroaromatic), 7.3-7.5 (aromatic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04232163
Source datasetuspto-grants-1980_11
ORD IDord-445ca06c839241da95e1f6d382f94a2a
Source noteuspto-grants-1980_11