Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1274997Generated: October 27, 2026

2-Chloro-N,N-dimethylpyrimidin-4-amine → N4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamine

https://huagongshe.com/reaction/1274997

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-N,N-dimethylpyrimidin-4-amineHCID 95975—
Reactant1-(2-Phenylethyl)piperidin-4-amineHCID 10728788—
SolventWaterHCID 962—
ProductN4,N4-dimethyl-N2-[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamineHCID 5392113128.4%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of 1-(2-phenylethyl)-4-piperidinamine (8.17 g) and 2-chloro-N,N-dimethyl-4-pyrimidinamine (6.3 g) was stirred for 20 hours at 120° C. The reaction mixture was diluted with water and extracted with CH2Cl2. The organic layer was washed with water, dried, filtered and the solvent evaporated. The residue was purified by column chromatography over silica gel (eluent: CH2Cl2 /CH3OH(NH3) 96/4). The pure fractions were collected and the solvent evaporated. The residue was crystallized from CH3CN. The precipitate was filtered off and dried, yielding 3.69 g (28.4%) of N4,N4 -dimethyl-N2 -[1-(2-phenylethyl)-4-piperidinyl]-2,4-pyrimidinediamine (comp. 11).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06159982
Source datasetuspto-grants-2000_12
ORD IDord-af6cd92b99fd43cf8bb49c0d311e7a2d
Source noteuspto-grants-2000_12