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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 25161Generated: October 29, 2026

N-bromobutanimide → Ethyl 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylate

https://huagongshe.com/reaction/25161

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-bromobutanimideHCID 67184—
ReactantEthyl pyrrolo[1,2-a]pyrazine-3-carboxylateHCID 22566021—
SolventDichloromethaneHCID 6344—
ProductEthyl 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylateHCID 2256574757%

Reaction Steps

To a solution of ethyl pyrrolo[1,2-a]pyrazine-3-carboxylate (0.60 g, 3.18 mmol) in CH2Cl2 (60 mL) is added N-bromosuccinimide (0.56 g, 3.18 mmol) in one portion. After 1 h, solvent is removed in vacuo and the crude solid purified using preparative HPLC (1% IPA/heptane (0-5 minutes) to 2% isocratic) to give a brown solid for ethyl 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylate. Yield 57%. MS (ESI+) for C10H9BrN2O2 m/z 271.01 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06858613B2
Source datasetuspto-grants-2005_02
ORD IDord-b27df28b5c5c442e933df3563681376d
Source noteuspto-grants-2005_02