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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1357539Generated: October 29, 2026

Aniline → 4-Anilino-2,5-dichloropyrimidine

https://huagongshe.com/reaction/1357539

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 8; 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 brine (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 numberUS06593326B1
Source datasetuspto-grants-2003_07
ORD IDord-99374a9e509d4110854883c8fff58f51
Source noteuspto-grants-2003_07