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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1013898Generated: October 31, 2026

4'-Mercaptoacetanilide → N-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-phenylpyrimidin-2-ylthio)phenyl)acetamide

https://huagongshe.com/reaction/1013898

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4'-MercaptoacetanilideHCID 70777—
Reactant(2-chloro-6-phenyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amineHCID 178418761—
Solventtert-ButanolHCID 6386—
ProductN-(4-(4-(5-methyl-1H-pyrazol-3-ylamino)-6-phenylpyrimidin-2-ylthio)phenyl)acetamideHCID 17841906185%

Reaction Steps

The above prepared (2-chloro-6-phenyl-pyrimidin-4-yl)-(5-methyl-2H-pyrazol-3-yl)-amine (60 mg, 0.21 mmol) is combined with 4-acetamidothiophenol (176 mg, 1.05 mmol) in tert-butanol (5 mL) and the mixture heated at reflux for 20 hours. The reaction mixture is cooled to room temperature and partitioned between ethyl acetate and aqueous NaHCO3. The organic layer is washed with brine, dried over MgSO4 and concentrated in vacuo. The resulting residue is purified by flash chromatography (SiO2, DCM/MeOH gradient) to afford [2-(4-acetamido-phenylsulfanyl)-6-phenyl-pyrimidin-4-yl]-(5-methyl-2H-pyrazol-3-yl)-amine (74 mg, 85%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982037B2
Source datasetuspto-grants-2011_07
ORD IDord-22f2c41db3ca4acfa23b8b027de31ba0
Source noteuspto-grants-2011_07