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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1611626Generated: November 1, 2026

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

https://huagongshe.com/reaction/1611626

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 numberUS06989385B2
Source datasetuspto-grants-2006_01
ORD IDord-c350f614ce0b4f1092a76e12b954c9ee
Source noteuspto-grants-2006_01