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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47625Generated: October 30, 2026

4-[[5-(3,5-dichloro-phenylsulfanyl)-1-isopropyl-3-methyl-1H-pyrazol-4-yl]-hydroxy-methyl]-pyridine → 4-[[5-(3,5-Dichlorophenyl)sulfanyl-1-isopropyl-3-methyl-pyrazol-4-yl]methyl]pyridine

https://huagongshe.com/reaction/47625

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-[[5-(3,5-dichloro-phenylsulfanyl)-1-isopropyl-3-methyl-1H-pyrazol-4-yl]-hydroxy-methyl]-pyridineHCID 10158344—
ReactantSodium BisulfiteHCID 23665763—
ReactantHCID 178506614HCID 178506614—
SolventBenzeneHCID 241—
Product4-[[5-(3,5-Dichlorophenyl)sulfanyl-1-isopropyl-3-methyl-pyrazol-4-yl]methyl]pyridineHCID 990851161.9%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of 466 mg of phosphorus tetraiodide in 15 mL of benzene was heated at 80° C. for 15 minutes. To this solution was added dropwise a solution of 400 mg of 4-[[5-(3,5-dichloro-phenylsulfanyl)-1-isopropyl-3-methyl-1H-pyrazol-4-yl]-hydroxy-methyl]-pyridine in 10 mL of benzene. The mixture was then heated at 80° C. for 1 hour then allowed to cool to room temperature. Then 8 mL of 10% aqueous sodium bisulphite solution was added and the biphasic mixture stirred for 1 hour. The aqueous phase was extracted three times with 30 mL of ethyl acetate and combined extracts were washed with brine, dried, filtered and evaporated to give a yellow residue which was purified by flash chromatography on silica gel using ethyl acetate/hexane (1:1 then 2:1) for the elution to give 238 mg of 4-[5-(3,5-dichloro-phenylsulfanyl)-1-isopropyl-3-methyl-1H-pyrazol-4-ylmethyl]-pyridine as a white solid. Mass spectrum (ES) m/z 392 [M+H]+, 433 [M+H+MeCN]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06699887B2
Source datasetuspto-grants-2004_03
ORD IDord-8cadc6e394c64badb59f552f2ce61f9c
Source noteuspto-grants-2004_03