HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 3-bromo-6-fluoro-1-methyl-1H-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 1H-Pyrrolo[2,3-b]pyridine, 6-fluoro-1-methyl- | HCID 67816521 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-bromo-6-fluoro-1-methyl-1H-pyrrolo[2,3-b]pyridine | HCID 67814018 | 99.4% |
Reaction Steps
To a solution of 6-fluoro-1-methyl-1H-pyrrolo[2,3-b]pyridine (257.3 g, 1.71 mol) in DCM (3.86 L) is added N-bromosuccinimide (320.3 g; 1.80 mol) in five portions over 30 minutes. The mixture is stirred without heating or cooling overnight, then filtered and concentrated to about 1 L. This is purified by column chromatography on silica, eluting with 0 to 30% EtOAc in isohexane. The appropriate fractions are evaporated to give the product as an off white solid (391.3 g, 1.7 mol). 1H-NMR (400 MHz, CDCl3): δ 7.91-7.87 (m, 1H), 7.15 (s, 1H), 6.77 (d, 1H), 3.81 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778946B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-b3138332b814421a862db043f80dcc3a |
| Source note | uspto-grants-2014_07 |