Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1463844Generated: November 3, 2026

Chloride → 1-(1-Naphthoyl)-3-[4-(5,6,7,8-tetrahydro-2-naphthyl)-2-thiazolyl]thiourea

https://huagongshe.com/reaction/1463844

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorideHCID 312—
Reactant1-Naphthoic acidHCID 6847—
ReactantAmmonium thiocyanateHCID 15666—
Reactant2-Amino-4-(5,6,7,8-tetrahydro-2-naphthyl)thiazoleHCID 735091—
CatalystDimethylformamideHCID 6228—
SolventAcetoneHCID 180—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product1-(1-Naphthoyl)-3-[4-(5,6,7,8-tetrahydro-2-naphthyl)-2-thiazolyl]thioureaHCID 1908874845.4%

Reaction Steps

DMF (1 drop) was added to a solution of 1-naphthoic acid (900 mg) in THF (10 ml), followed by addition of oxayly chloride (0.49 ml) and stirring at room temperature for 2 hours. After replacing the solvent with acetone (10 ml), a solution of ammonium thiocyanate (436 mg) in acetone (5 ml) was added to the solution, followed by heating over a warm water bath for 1 minute and stirring at room temperature for 20 minutes. Then, a solution of 2-amino-4-(5,6,7,8-tetrahydro-2-naphthyl)thiazole (1,00 g) in acetone (10 ml) was added to the mixed solution, which was then stirred at room temperature for 16 hours. The reaction solution was poured into water, and the crystals which separated out were recovered by filtration and washed with diethyl ether. Recrystallization from dichloroethane-ethanol produced 1-(1-naphthoyl)-3-[4-(5,6,7,8-tetrahydro-2-naphthyl)-2-thiazolyl]thiourea (yield of 875 mg, 45.4%) in the form of colorless needles. m.p. 216°-217° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05302608
Source datasetuspto-grants-1994_04
ORD IDord-191cd670c6804b1ead7a1d542bb0b7f9
Source noteuspto-grants-1994_04