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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416042Generated: November 1, 2026

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

https://huagongshe.com/reaction/1416042

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Imidazole-2-methanol, 5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-1-((4-nitrophenyl)methyl)-HCID 474029—
ReactantHCID 178418361HCID 178418361—
CatalystPlatinumHCID 23939—
SolventEthyl AcetateHCID 8857—
Product1H-Imidazole-2-methanol, 1-((4-aminophenyl)methyl)-5-((3,5-dichlorophenyl)thio)-4-(1-methylethyl)-HCID 47403078%

Reaction Steps

In ethyl acetate was dissolved 800 mg of 5-(3,5-dichlorophenylthio)-2-hydroxymethyl-4-isopropyl-1-(p-nitrobenzyl)-1H-imidazole (103a), and platinum sulfided carbon was added. After replacement with hydrogen atomosphere, the mixture was catalytically hydrogenated under atmospheric pressure at room temperatures After 1 hour, the mixture was filtered through Celite, the filtrate was distilled off under reduced pressure, and to the residue, diethyl ether was added. The precipitated crystals were filtered, and 579 mg of 1-(p-aminobenzyl)-5-(3,5-dichlorophenylthio)-2-hydroxymethyl-4-isopropyl-1H-imidazole (104a)was obtained (yield 78%). mp 130° C. (decomp.)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05910506
Source datasetuspto-grants-1999_06
ORD IDord-bb3f760ac37a4cd7855b5f725bd2cf2a
Source noteuspto-grants-1999_06