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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1720762Generated: November 2, 2026

Pyridine → 1-(5-Methyl-4-phenyl-4H-1,2,4-triazol-3-yl)piperazine

https://huagongshe.com/reaction/1720762

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantPiperazineHCID 4837—
ReactantHCID 12217059HCID 12217059—
SolventDichloromethane methanolHCID 21226129—
Product1-(5-Methyl-4-phenyl-4H-1,2,4-triazol-3-yl)piperazineHCID 22418762—

Reaction Steps

A mixture of 3-bromo-5-methyl-4-phenyl-4H-1,2,4-triazole (4.16 g), 15.07 g of piperazine and 20 ml of pyridine is stirred at 100° under nitrogen for 22 h. The reaction is monitored by TLC (8% methanol/methylene chloride) and after this period of time no change occurs. The mixture is subsequently placed in a Parr bomb and heated in an oil bath at 180° for 24 h. Bomb pressure increases by 40 psi. The mixture is worked up by partitioning between chloroform and water. The organic phase is washed with saturated aqueous sodium bicarbonate (2×) and with saline (2×), dried over sodium sulfate and concentrated to a solid, the product is recrystallized in ethyl acetate, MS [M+H]+ 243.1484

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05506354
Source datasetuspto-grants-1996_04
ORD IDord-170b2d12565145f5a11c9ef827bea9b7
Source noteuspto-grants-1996_04