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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 399629Generated: October 31, 2026

Triethylamine → 4-(2,4-dichlorophenyl)-5-methyl-2-[N-(alpha-cyclopropyl-4-bromobenzyl)-N-propylamino]thiazole

https://huagongshe.com/reaction/399629

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Bromo-1-(2,4-dichlorophenyl)propan-1-oneHCID 10923991—
ReactantN-(alpha-cyclopropyl-4-bromobenzyl)-N-propylthioureaHCID 18967805—
SolventEthanolHCID 702—
Product4-(2,4-dichlorophenyl)-5-methyl-2-[N-(alpha-cyclopropyl-4-bromobenzyl)-N-propylamino]thiazoleHCID 15291608—

Reaction Conditions

Temperature65 °C

Reaction Steps

14 g of 2-bromo-1-(2,4-dichlorophenyl)-1-propanone (Compound 1), 17.1 g of N-(α-cyclopropyl-4-bromobenzyl)-N-propylthiourea (Compound 64) and 7.6 ml of triethylamine are dissolved in 200 ml of ethanol and the solution is heated to 65° C. The reaction is monitored by TLC. At the end of the reaction, the ethanol is removed and the residue is hydrolysed with water and extracted with methylene chloride. The organic phases are washed and dried. The product is purified on a column of silica, using a mixture of cyclohexane and ethyl acetate (20:1 v/v) as eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05821255
Source datasetuspto-grants-1998_10
ORD IDord-41160342b3da4f80b92077bc9f490998
Source noteuspto-grants-1998_10