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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045749Generated: October 30, 2026

Formaldehyde → 5-Bromo-2-methyl-8-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazine

https://huagongshe.com/reaction/1045749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFormaldehydeHCID 712—
ReactantDichloromethaneHCID 6344—
ReactantSodium BicarbonateHCID 516892—
Reactant5-Bromo-2-methyl-8-(piperazin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazineHCID 58447057—
SolventMethanolHCID 887—
Product5-Bromo-2-methyl-8-(4-methylpiperazin-1-yl)-[1,2,4]triazolo[1,5-a]pyrazineHCID 5844698476%

Reaction Steps

A 100 mL round bottom flask was charged with 5-bromo-2-methyl-8-(piperazin-1-yl)-[1,2,4]-triazolo[1,5-a]pyrazine (0.5 g, 1.7 mmol), CH2Cl2 (20 mL), MeOH (10 mL), 40% aqueous formaldehyde (2 mL) and NaBH3(CN) (0.5 g, 8.0 mmol). The resulting solution was stirred at room temperature for 0.5 h. Work-up: the reaction mixture was poured into saturated aqueous NaHCO3 and extracted with CH2Cl2 (50 mL×3). The combined organic layers were dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with 1-10% MeOH in CH2Cl2, to afford 0.4 g (76%) of the product as a yellow solid. MS m/z: 311 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569300B2
Source datasetuspto-grants-2013_10
ORD IDord-7e7f697cf5fe49378143303cecd53064
Source noteuspto-grants-2013_10