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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 80564Generated: October 27, 2026

Methyl N-{5-bromo-3-[(2-chloro-3,6-difluorobenzyl)amino]pyrazin-2-yl}-beta-alaninate → 3-bromo-5-(2-chloro-3,6-difluorobenzyl)-5,7,8,9-tetrahydro-6H-pyrazino[2,3-b][1,4]diazepin-6-one

https://huagongshe.com/reaction/80564

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl N-{5-bromo-3-[(2-chloro-3,6-difluorobenzyl)amino]pyrazin-2-yl}-beta-alaninateHCID 86659427—
SolventAcetic AcidHCID 176—
Product3-bromo-5-(2-chloro-3,6-difluorobenzyl)-5,7,8,9-tetrahydro-6H-pyrazino[2,3-b][1,4]diazepin-6-oneHCID 86659429—

Reaction Steps

A solution of methyl N-{5-bromo-3-[(2-chloro-3,6-difluorobenzyl)amino]pyrazin-2-yl}-β-alaninate in HOAc was heated at reflux for 4 hrs. After volatile components were removed on rotavap, the residue was taken in to a mixture of EtOAc and aq. NaHCO3. The combined organic layers from extraction was dried, concentrated, and then purified by silica gel column chromatography (EtOAc/Hexanes 4:1) to furnish 3-bromo-5-(2-chloro-3,6-difluorobenzyl)-5,7,8,9-tetrahydro-6H-pyrazino[2,3-b][1,4]diazepin-6-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846664B2
Source datasetuspto-grants-2014_09
ORD IDord-804ef3f1b16e432d861abd94f5563870
Source noteuspto-grants-2014_09