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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 720728Generated: October 30, 2026

Water → 2-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-5-methanesulfonyl-pyridine

https://huagongshe.com/reaction/720728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2-Hydrazino-5-(methanesulfonyl)-pyridineHCID 9964293—
ReactantN-(1-ethoxy-ethylidene)-4-bromo-benzamideHCID 21894671—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product2-[5-(4-Bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-5-methanesulfonyl-pyridineHCID 1019417861.1%

Reaction Steps

N-(1-ethoxy-ethylidene)-4-bromo-benzamide 565 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, (5-methansulfonyl-pyridine-2-yl)-hydrazine 431 mg(2.23 mmol) was added to the solution and the solution was stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane, and then, the collected organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was re-crystallized in acetone and hexane phase. As a result, 2-[5-(4-bromo-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-5-methanesulfonyl-pyridine (502 mg, yield: 61%) was obtained as a solid phase.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07135572B2
Source datasetuspto-grants-2006_11
ORD IDord-dcc5f80b083447549940b60c3f099c05
Source noteuspto-grants-2006_11