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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1857750Generated: October 31, 2026

Water → 1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-(3-(2-pyridinyl)propyl)-, carbamate

https://huagongshe.com/reaction/1857750

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantTrichloroacetyl isocyanateHCID 76400—
ReactantHCID 474135HCID 474135—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-(3-(2-pyridinyl)propyl)-, carbamateHCID 47404883%

Reaction Conditions

Temperature-40 °C

Reaction Steps

In 10 ml of tetrahydrofuran was dissolved 110 mg of 5-(3,5-dichlorophenylthio)-4-isopropyl-2-hydroxymethyl-1-(3-(2-pyridyl)propyl)-1H-imidazole, and the mixture was cooled to -40° C. Under stirring, 45.1 μl of trichloroacetylisocyanate was added, the mixture was allowed to warm up to room temperature, and stirred for 30 minutes. Added were 100 μl of triethylamine, 600 μl of water and 600 μl of methanol, and the mixture was stirred at 70° C. for 1 hour. After completion of the reaction, the solution was distilled off under reduced pressure, an aqueous sodium hydrogen carbonate solution was added, extracted with ethyl acetate, the extract was dried over sodium sulfate, and the solvent was distilled off under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate:methanol=10:1) to give 80 mg of Compound I-130 (yield 83%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06147097
Source datasetuspto-grants-2000_11
ORD IDord-7a7ac9f0e1ae42eebd8aa1b7cbe054b3
Source noteuspto-grants-2000_11