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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416044Generated: November 1, 2026

1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-((3-nitrophenyl)methyl)- → 1H-Imidazole-2-methanol, 1-((3-aminophenyl)methyl)-5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-

https://huagongshe.com/reaction/1416044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-((3-nitrophenyl)methyl)-HCID 474032—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
Product1H-Imidazole-2-methanol, 1-((3-aminophenyl)methyl)-5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-HCID 474033—

Reaction Steps

In ethyl acetate was dissolved 64 mg of 5-(3,5-dichlorophenylthio)-2-hydroxymethyl-4-isopropyl-1-(m-nitrobenzyl)-1H-imidazole (103b), and platinum sulfided carbon was added. After replacement with hydrogen atomosphere, the mixture was catalytically hydrogenated under atmospheric pressure at room temperature. After 3 hours, the mixture was filtered through Celite, the filtrate was distilled off under reduced pressure, and diethyl ether was added. Crystals precipitated were filtered, and 25 mg of Compound I-118 was obtained (yield 42%). mp 145-148° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910506
Source datasetuspto-grants-1999_06
ORD IDord-9bc3056dc16a46518d2321d0f0867119
Source noteuspto-grants-1999_06