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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349422Generated: October 26, 2026

Diisopropylethylamine → N-(3-Amino-4-thienyl)-N'-(2-trifluoromethylphenyl)thiourea

https://huagongshe.com/reaction/349422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Trifluoromethyl)phenyl isothiocyanateHCID 737162—
ReactantThiophene-3,4-diamine dihydrobromideHCID 21989329—
SolventTetrahydrofuranHCID 8028—
ProductN-(3-Amino-4-thienyl)-N'-(2-trifluoromethylphenyl)thioureaHCID 86037742—

Reaction Steps

0.8 g of 3,4-diaminothiophene dihydrobromide was added to a mixture of 0.74 g of N-ethyl-N,N-diisopropylamine in 40 ml of anhydrous THF, and the mixture was stirred at room temperature for 10 minutes, and then admixed with 0.58 g of 2-trifluoromethylphenyl isothiocyanate. The mixture was stirred at room temperature for 3 hours and at 40° C. for a further 10 minutes, and left to stand at room temperature overnight. After the solvent had been distilled off, the residue was admixed with water and extracted with ethyl acetate, and the insoluble fraction was filtered off. The organic phase was washed with water and dried over sodium sulfate, the solvent was distilled off and the residue was purified by column chromatography on silica gel using a mixture of 1 part by volume of toluene and 1 part by volume of ethyl acetate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179830B2
Source datasetuspto-grants-2007_02
ORD IDord-7e922d213da34423aab1dbbb22c3a97f
Source noteuspto-grants-2007_02