HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Ethyl 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl pyrrolo[1,2-a]pyrazine-3-carboxylate | HCID 22566021 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 6-bromopyrrolo[1,2-a]pyrazine-3-carboxylate | HCID 22565747 | 57% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06858613B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-b27df28b5c5c442e933df3563681376d |
| Source note | uspto-grants-2005_02 |