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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522524Generated: October 31, 2026

N-bromobutanimide → Methyl 3-Amino-6-bromopyrazine-2-carboxylate

https://huagongshe.com/reaction/522524

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 3-aminopyrazinecarboxylateHCID 72669—
SolventAcetonitrileHCID 6342—
ProductMethyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 22725192.3%

Reaction Steps

A mixture of methyl 3-aminopyrazine-2-carboxylate (8.35 g, 54.53 mmol) and N-bromo-succinimide (9.705 g, 54.53 mmol) was stirred in MeCN (100 mL) at RT for 16 hours. The resultant precipitate was filtered, washed with MeCN and dried to give the desired product as a yellow solid (11.68 g, 92% Yield) 1H NMR (400.0 MHz, DMSO) δ 3.85 (s, 3H), 7.55 (br s, 2H) and 8.42 (s, 1H) ppm; MS (ES+) 233.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334244B2
Source datasetuspto-grants-2016_05
ORD IDord-059c3b3caa014724bd242a7ad3aed591
Source noteuspto-grants-2016_05