HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 6-Bromo-7-azaindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Benzoyl-6-bromo-7-azaindole | HCID 15013893 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 6-Bromo-7-azaindole | HCID 11159915 | 95% |
Reaction Steps
A solution of 1-benzoyl-6-bromo-1H-pyrrolo[2,3-b]pyridine (0.046 g, 0.15 mmol) in methanol (5.0 mL) was added with 5 N aqueous sodium hydroxide (1.0 mL), and the mixture was stirred at room temperature for 2 hours. The solvent was evaporated under reduced pressure, the residue was extracted with diethyl ether, and then the organic layer was washed successively with water and saturated brine, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure to obtain 6-bromo-1H-pyrrolo[2,3-b]pyridine (0.028 g, 95%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09156827B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-fcaa67e39a4f4393b407b84726845077 |
| Source note | uspto-grants-2015_10 |