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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577389Generated: October 25, 2026

Sodium Hydroxide → 3-Chloro-4-[(2-chloropyrimidin-4-yl)thio]-2-methylaniline

https://huagongshe.com/reaction/577389

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant2,4-DichloropyrimidineHCID 77531—
ReactantSodium borohydrideHCID 4311764—
ReactantSodium hydrosulfide hydrateHCID 16211346—
Reactant3-Chloro-2-methyl-4-thiocyanatoanilineHCID 37859309—
SolventMethanol--water (1/1)HCID 22242641—
Product3-Chloro-4-[(2-chloropyrimidin-4-yl)thio]-2-methylanilineHCID 5949167441.1%

Reaction Conditions

Temperature0 °C

Reaction Steps

Crude 4-amino-2-chloro-3-methylphenyl thiocyanate (600 mg, 3.0 mmol) was dissolved in a mixture of methanol:water (2:1, 22 mL) and cooled to 0° C. Sodium hydrosulfide monohydrate (338 mg, 4.6 mmol) and sodium borohydride (447 mg, 11.8 mmol) were added then the mixture was allowed to warm to room temperature and stir overnight. After this time sodium hydroxide (96 mg, 2 4 mmol) was added followed by 2,4-dichloropyrimidine (360 mg, 2 4 mmol) and the mixture allowed to stir for a further 24h. The methanol was removed in vacuo and then the mixture was extracted with ethyl acetate. The extracts were dried (Na2SO4) and evaporated then the residue was purified by flash chromatography to afford 3-chloro-4-[(2-chloropyrimidin-4-yl)thio]-2-methylaniline (353 mg, 41%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09040549B2
Source datasetuspto-grants-2015_05
ORD IDord-bdf6316b2b9347548381cd6d76757d55
Source noteuspto-grants-2015_05