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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 63108Generated: October 29, 2026

(4-Methylpyridin-2-yl)methanamine → N4-cyclohexyl-5,6-dimethyl-N2-[(4-methylpyridin-2-yl)methyl]pyrimidine-2,4-diamine

https://huagongshe.com/reaction/63108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(4-Methylpyridin-2-yl)methanamineHCID 15144432—
ReactantN4-cyclohexyl-5,6-dimethyl-N2-(pyridin-2-ylmethyl)pyrimidine-2,4-diamine hydrochlorideHCID 131737202—
ProductN4-cyclohexyl-5,6-dimethyl-N2-[(4-methylpyridin-2-yl)methyl]pyrimidine-2,4-diamineHCID 71738337—

Reaction Steps

The titled compound was synthesized according to the general procedure described for preparation of N4-cyclohexyl-5,6-dimethyl-N2-(pyridin-2-ylmethyl)pyrimidine-2,4-diamine (Example 1) using (4-methylpyridin-2-yl)methanamine instead of (pyridin-2-ylmethyl)amine. The product was purified by column chromatography eluting with mixture of chloroform/ethanol/20% water solution of ammonia (200:10:1), and then the final product was washed with diethyl ether to afford the titled compound as a light-grey solid. 1H NMR (300 MHz, DMSO-d6) δ ppm 0.92-1.67 (m, 10H), 1.88 (s, 3H), 2.28 (s, 3H), 2.53 (s, 3H), 3.63 (bs, 1H), 4.92 (d, J=4.30 Hz, 2H), 7.60-7.80 (m, 3H), 8.19 (bs, 1H), 8.66 (d, J=5.64 Hz, 1H), 13.34 (s, 1H); MS (ESI) m/z 326.0 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447051B2
Source datasetuspto-grants-2016_09
ORD IDord-644c41c40e514b22aed100b4c55e06b8
Source noteuspto-grants-2016_09