Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748644Generated: October 30, 2026

Phenyl thioxochloroformate → 4-[(4-Chloroindol-1-yl)methyl]-1,3-dihydroimidazole-2-thione

https://huagongshe.com/reaction/748644

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenyl thioxochloroformateHCID 70498—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(4-Chloro-indol-1-ylmethyl)-1,3-dihydro-imidazoleHCID 69203960—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-[(4-Chloroindol-1-yl)methyl]-1,3-dihydroimidazole-2-thioneHCID 1160863450%

Reaction Steps

4-(4-Chloro-indol-1-ylmethyl)-1,3-dihydro-imidazole (Intermediate A4) (0.5 mmol) in THF (3 mL) and water (3 mL) was treated with NaHCO3 (5 mmol) at rt for 20 m. Phenyl chlorothionoformate (1.3 mmol) was added and stirring was continued for 4 h. The mixture was diluted with water (15 mL) and extracted with ether (3×25 mL). The organic portions were combined, dried over MgSO4, filtered and the solvent was removed under vacuum. The residue was dissolved in MeOH (4 mL) and treated with NEt3 (0.35 mL) for 18 h at rt. The solvent was evaporated and the product was washed on a glass frit with 50% CH2Cl2:hexanes to give a solid 4-(4-chloro-indol-1-ylmethyl)-1,3-dihydro-imidazole-2-thione (Compound 1) (˜50%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399868B2
Source datasetuspto-grants-2008_07
ORD IDord-90db86b23eb34d44a2f2e3b1139be000
Source noteuspto-grants-2008_07