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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 711380Generated: October 27, 2026

Tert-butyl 4-(2-(7-bromoquinoxalin-2-yl)hydrazinecarbonyl)piperidine-1-carboxylate → 8-Bromo-1-(piperidin-4-yl)[1,2,4]triazolo[4,3-a]quinoxaline

https://huagongshe.com/reaction/711380

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-(7-bromoquinoxalin-2-yl)hydrazinecarbonyl)piperidine-1-carboxylateHCID 66803410—
SolventAcetic AcidHCID 176—
Product8-Bromo-1-(piperidin-4-yl)[1,2,4]triazolo[4,3-a]quinoxalineHCID 6680326783%

Reaction Steps

A mixture of tert-butyl 4-(2-(7-bromoquinoxalin-2-yl)hydrazinecarbonyl)piperidine-1-carboxylate (900 mg, 2.0 mmol) in AcOH (10 mL) was refluxed overnight. Then the solvent was removed, and the residue was purified by ISCO (MeOH/H2O=20%-90%) to afford 8-bromo-1-(piperidin-4-yl)[1,2,4]triazolo[4,3-a]quinoxaline as a pale yellow solid (550 mg, yield 83.0%). MS (m/z): 332 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181264B2
Source datasetuspto-grants-2015_11
ORD IDord-08daaeac9458446798f911c1381b3226
Source noteuspto-grants-2015_11