HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-Difluoro-3-nitrobenzoyl chloride → (2,6-difluoro-3-nitrophenyl)(5-iodo-1H-pyrrolo[2,3-b]pyridin-3-yl)methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-Difluoro-3-nitrobenzoyl chloride | HCID 2781756 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | 5-Iodo-1H-pyrrolo[2,3-b]pyridine | HCID 24229214 | — |
| Solvent | Nitromethane | HCID 6375 | — |
| Product | (2,6-difluoro-3-nitrophenyl)(5-iodo-1H-pyrrolo[2,3-b]pyridin-3-yl)methanone | HCID 58368945 | 60.2% |
Reaction Steps
In a reaction vial, 5-iodo-1H-pyrrolo[2,3-b]pyridine (43, 1.00 g, 4.10 mmol) is mixed with 22 mL of nitromethane and aluminum trichloride (3.28 g, 24.6 mmol) is added. The reaction is stirred at room temperature for 1 hour and 2,6-difluoro-3-nitro-benzoyl chloride (44, 1.36 g, 6.15 mmol) is added. The reaction is heated at 45° C. for 93 hours, then quenched with addition of methanol. The resulting precipitate is collected by filtration to provide the desired compound (45, 1.06 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09440969B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-782eadf38732454696f9145acdc86ea2 |
| Source note | uspto-grants-2016_09 |