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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204797Generated: October 30, 2026

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

https://huagongshe.com/reaction/2204797

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 room temp overnight. 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) 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 numberUS09365557B2
Source datasetuspto-grants-2016_06
ORD IDord-07be5df3023e4aa2974e1a3567427ce4
Source noteuspto-grants-2016_06