Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1937415Generated: November 1, 2026

Benzyl Chloride → N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine

https://huagongshe.com/reaction/1937415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl ChlorideHCID 7503—
ReactantTriethylamineHCID 8471—
ReactantN2,N4,N4-trimethyl-N2-(4-piperidinyl)-2,4-pyrimidinediamineHCID 53854017—
SolventDimethylacetamideHCID 31374—
ProductN2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamineHCID 5706698655.4%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of chloromethylbenzene (1.9 g), intermediate 2 (3 g) and triethylamine (2.62 g) in N,N-dimethylacetamide (55 ml) was stirred for 2 hours at 75° C. The reaction mixture was poured out into ice-water and extracted with toluene. The separated organic layer was washed three times with water, dried, filtered and the solvent evaporated. The residue was dissolved in boiling petroleum ether and treated with activated charcoal. The mixture was filtered warm over dicalite, and the filtrate was concentrated. The concentrate was cooled on an ice-bath and the resulting precipitate was filtered off and dried, yielding 2.3 g (54.4%) of N2,N4,N4-trimethyl-N2-[1-(phenylmethyl)-4-piperidinyl]-2,4-pyrimidinediamine (comp. 8).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06395742B1
Source datasetuspto-grants-2002_05
ORD IDord-39e5f7c0c7a04a6b8f610113f81985dc
Source noteuspto-grants-2002_05