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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 646662Generated: October 31, 2026

Sodium Carbonate → Methyl 3-Amino-6-bromopyrazine-2-carboxylate

https://huagongshe.com/reaction/646662

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantBromineHCID 24408—
ReactantMethyl 3-aminopyrazinecarboxylateHCID 72669—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductMethyl 3-Amino-6-bromopyrazine-2-carboxylateHCID 22725191%

Reaction Steps

Commercially available methyl 3-amino-pyrazine-2-carboxylate (available from Aldrich Chemical Company) was brominated using a procedure similar to that of Russ, T., Ried, W., Ullrich, F., and Mutschler, E. Arch. Pharm. (Weinheim) 1992, 325, 761-767. To a solution of methyl 3-amino-2-pyrazine carboxylate (30.0 g, 200 mmol) in acetic acid (200 mL), bromine (11 mL) was added slowly via addition funnel. After complete addition of bromine, sodium carbonate powder was added slowly until precipitation occurred. The reaction mixture was allowed to stir at room temperature for 2 h. The reaction mixture was reduced to half-volume in vacuo and then diluted with water (500 mL). The reaction mixture was shaken vigorously and the resulting solid was collected using vacuum filtration. The solid was washed with ether to afford a pure yellow solid (91% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07704995B2
Source datasetuspto-grants-2010_04
ORD IDord-ad1be0b34c60482eb7d55180ee66c6de
Source noteuspto-grants-2010_04