HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Iodosuccinimide → 2-bromo-7-iodo-5H-pyrrolo(2,3-b)pyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-bromo-5H-pyrrolo[2,3-b]pyrazine | HCID 25067308 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 2-bromo-7-iodo-5H-pyrrolo(2,3-b)pyrazine | HCID 44118277 | — |
Reaction Steps
To a solution of 2-Bromo-5H-pyrrolo[2,3-b]pyrazine (258 mg, 1.3 mmol) in acetone (5 ml) was added N-iodosuccinimide (324 mg, 1.44 mmol) in one portion. The reaction mixture was stirred at room temperature for 45 minutes. The resulting precipitate was filtered off, washed with a minimal amount of acetone, and dried in vacuum to give the title compound as a light brown solid 1H-NMR (500 MHz, d6-DMSO) δ 12.81 (s br, 1H), 8.40 (s, 1H), 8.19 (d, 3.0 Hz, 1H). MS: m/z 323.8/325.8 [MH+].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08268994B2 |
| Source dataset | uspto-grants-2012_09 |
| ORD ID | ord-2bc46f13a6c54adc8bcbc0ab470f0849 |
| Source note | uspto-grants-2012_09 |