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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1830589Generated: November 2, 2026

Aniline → 5-bromo-2-chloro-N-phenylpyrimidin-4-amine

https://huagongshe.com/reaction/1830589

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2,4-dichloropyrimidineHCID 289973—
Solvent1-ButanolHCID 263—
Product5-bromo-2-chloro-N-phenylpyrimidin-4-amineHCID 11403389—

Reaction Steps

A solution of 5-bromo-2,4-dichloropyrimidine (6.84 g, 30.0 mmol), aniline (2.79 g, 30.0 mmol) and N,N-diisopropylethylamine (3.87 g, 30.0 mmol) in n-butanol (75 ml) was heated under relux for 4 hours. Volatile material was removed by evaporation and the residue was dissolved in DCM (100 ml). The solution was washed with water (3×100 ml) and saturated brine (100 ml) and dried. Volatile material was removed by evaporation and the residue was purified by column chromatography, eluting with 15% ethyl acetate/isohexane, to give the product as an oil which solidifed on standing (5.12 g, 60%). NMR: 7.1 (t, 1H), 7.4 (t, 2H), 7.55 (d, 2H), 8.4 (s, 1H), 9.2 (br s, 1H); MS (MH+): 284, 286, 288.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067522B2
Source datasetuspto-grants-2006_06
ORD IDord-6441fc37475c47e8830a3471f95e11c5
Source noteuspto-grants-2006_06