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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480015Generated: October 31, 2026

Aniline → 4-Anilino-2,5-dichloropyrimidine

https://huagongshe.com/reaction/480015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantDiisopropylethylamineHCID 81531—
Reactant2,4,5-TrichloropyrimidineHCID 237259—
Solvent1-ButanolHCID 263—
Product4-Anilino-2,5-dichloropyrimidineHCID 18768047—

Reaction Steps

A solution of 2,4,5-trichloropyrimidine (Method 3; 5.5 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 reflux 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 sodium chloride solution (100 ml) and dried. Volatile material was removed by evaporation and the residue was purified by column chromatography on silica gel, eluting with 15% ethyl acetate/isohexane, to give the product as an oil which solidified on standing (3.94 g, 54%). NMR: 7.2 (t, 1H), 7.4 (t, 2H), 7.6 (d, 2H), 8.4 (s, 1H), 9.45 (br s, 1H); MS (MH+): 240, 242, 244.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06649608B2
Source datasetuspto-grants-2003_11
ORD IDord-255e95f1f4734a1f9bf21843ae19c96f
Source noteuspto-grants-2003_11