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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 989707Generated: October 26, 2026

Pentylamine → N-(2-Amino-5-benzyl-6-methylpyrimidine-4-yl)-N-pentylamine

https://huagongshe.com/reaction/989707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPentylamineHCID 8060—
Reactant5-Benzyl-4-chloro-6-methylpyrimidin-2-amineHCID 820238—
Solvent1,4-DioxaneHCID 31275—
ProductN-(2-Amino-5-benzyl-6-methylpyrimidine-4-yl)-N-pentylamineHCID 1204376389.7%

Reaction Steps

A mixture of 5-benzyl-4-chloro-6-methylpyrimidine-2-ylamine (500 mg, 2.14 mmol) , amylamine (1.24 ml ) and dioxane (4 ml ) was kept at 95-100° C. for 19 hours. The reaction mixture was concentrated in vacuo, and the residue was extracted with chloroform and a saturated aqueous NaHCO3 solution. The organic layer was washed with saturated brine, dried over sodium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography (2%MeOH/CHCl3) to give the object compound (546 mg, 89.7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06458798B1
Source datasetuspto-grants-2002_10
ORD IDord-0c51ed97379a4340923c28e477daca0e
Source noteuspto-grants-2002_10