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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1769513Generated: October 29, 2026

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

https://huagongshe.com/reaction/1769513

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 numberUS05380841
Source datasetuspto-grants-1995_01
ORD IDord-60fa16674c284a4da762026f25e8c7c0
Source noteuspto-grants-1995_01