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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2201570Generated: October 26, 2026

Bromine → 3-Amino-6-bromopyrazine-2-carboxamide

https://huagongshe.com/reaction/2201570

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromineHCID 24408—
ReactantAminopyrazine carboxamideHCID 280292—
ReactantSodium AcetateHCID 517045—
SolventAcetic AcidHCID 176—
Product3-Amino-6-bromopyrazine-2-carboxamideHCID 47089995%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred solution of 3-aminopyrazine-2-carboxamide (1 g, 7.24 mmol, prepared according to International Patent Application Publication No. WO2011054922) and NaOAc (200 mg, 2.44 mmol) in HOAc (15 mL) was added Br2 (0.45 mL) dropwise at 0° C. for 1 hour, and then it was stirred at 50° C. for 8 hours. After the mixing, it was poured into ice-water and filtrated, the crude product of 3-amino-6-bromopyrazine-2-carboxamide as brown solid (1.5 g, yield: 95%) was obtained. 1H-NMR (DMSO-d6, 400 MHz) δ 8.30 (s, 1H), 7.93 (s, 2H), 7.66 (s, 2H). MS (M+H)+: 217/219.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09364482B2
Source datasetuspto-grants-2016_06
ORD IDord-2a914bcbf20e4df0a7dbaf10d9f167cb
Source noteuspto-grants-2016_06