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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2294043Generated: October 25, 2026

Triethylamine → 5-(4-phenyl-3,6-dihydro-2H-pyridin-1-ylmethyl)-pyrimidine-2,4-diamine

https://huagongshe.com/reaction/2294043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-Phenyl-1,2,3,6-tetrahydropyridine hydrochlorideHCID 2723860—
Reactant5-(Bromomethyl)pyrimidine-2,4-diamine dihydrobromideHCID 21473608—
SolventDimethylformamideHCID 6228—
Product5-(4-phenyl-3,6-dihydro-2H-pyridin-1-ylmethyl)-pyrimidine-2,4-diamineHCID 2147361656.4%

Reaction Steps

A solution of 1.0 g (0.0051 mol) of 4-phenyl-1,2,3,6-tetrahydro-pyridine hydrochloride in 40 ml of dimethylformamide was treated with 2.13 ml (0.0153 mol) of triethylamine and 0.62 g (0.00170 mol) of 5-bromomethyl-pyrimidine-2,4-diamine dihydrobromide and the mixture was stirred at room temperature under argon for 65 hours. The mixture was completely freed from the solvents. The residue was chromatographed over silica with methanol as the eluent, digested in dichloromethane/water 1:1 and subsequently filtered off under suction. The organic phase was then completely freed from the solvents and the residue was digested in diethyl ether and subsequently filtered off under suction. A total of 0.27 g (56%) of 5-(4-phenyl-3,6-dihydro-2H-pyridin-1-ylmethyl)-pyrimidine-2,4-diamine was obtained as white crystals; m.p. 239°-241°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05688798
Source datasetuspto-grants-1997_11
ORD IDord-77b7b079e78243e3a1c13ae9df8d246e
Source noteuspto-grants-1997_11