HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 3-Bromo-1-(2-ethoxy naphthoyl)-7-azaindole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-Naphthalenecarbonyl chloride, 2-ethoxy- | HCID 108679 | — |
| Reactant | 3-Bromo-1H-pyrrolo[2,3-b]pyridine | HCID 5523659 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-Bromo-1-(2-ethoxy naphthoyl)-7-azaindole | HCID 49758913 | 101.2% |
Reaction Steps
3-Bromo-7-azaindole (500 mg, 2.0 mmol) 3 was dissolved in N,N-dimethylformamide (50 mL) and sodium hydride (210 mg, 5.3 mmol, 60% dispersion in mineral oil) and 2-Ethoxy-naphthalene-1-carbonyl chloride (710 mg, 3.0 mmol) were added. The reaction mixture was stirred at ambient temperature for 30 min, cast into ice water (100 mL) and extracted into ethyl acetate. The organic portion was dried with anhydrous magnesium sulfate, filtered and the filtrate concentrated. Purification via column chromatography (10% Ethyl acetate in hexanes) provided the desired product 85 (800 mg, 80%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07605168B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-714e4e7384fb4777baa087d810809a8a |
| Source note | uspto-grants-2009_10 |