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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1831620Generated: November 1, 2026

2,4,6-Trimethylaniline → N-Butyl-N-ethyl-2-methyl-5-ethyl-N'-(2,4,6-trimethylphenyl)-pyrimidine-4,6-diamine

https://huagongshe.com/reaction/1831620

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylanilineHCID 6913—
ReactantButyl-(6-chloro-2-methyl-5-ethyl-pyrimidin-4-yl)-ethylamineHCID 21912129—
ProductN-Butyl-N-ethyl-2-methyl-5-ethyl-N'-(2,4,6-trimethylphenyl)-pyrimidine-4,6-diamineHCID 21912156209.4%

Reaction Steps

A mixture of butyl-(6-chloro-2-methyl-5-ethyl-pyrimidin-4-yl)-ethylamine (200 mg, 0.78 mmol) and 2,4,6-trimethylaniline (0.963 g, 7.1 mmol) was heated at reflux for 4 hours. The mixture was quenched with water and extracted with ethyl acetate. The organic layer was washed with saturated potassium carbonate and brine, dried and concentrated to give a dark oil. The oil was distilled to give 579 mg of the dark oil which was then purified through silica gel column chromatography using chloroform as eluent to give the title compound as a brown oil. 1H NMR (CDCl3) δ 0.93 (t, 3H), 1.14 (t, 3H), 1.1–1.4 (m, 4H), 1.45–1.60 (m, 2H), 2.17 (s, 6H), 2.30 (s, 3H), 2.33 (s, 3H), 3.2–3.4 (m, 4H), 6.90 (s, 2H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07067664B1
Source datasetuspto-grants-2006_06
ORD IDord-abfe8e5e46e146348b952f8f9e096359
Source noteuspto-grants-2006_06