HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine → 6-Methyl-1H-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine | HCID 49759033 | — |
| Reactant | HCID 178477797 | HCID 178477797 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 6-Methyl-1H-pyrrolo[2,3-b]pyridine | HCID 11457716 | 88% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of methylzinc chloride in THF (2 M) (9 mL, 12 mmol) was added to 6-chloro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (0.600 g, 2.05 mmol) and Pd(PPh3)4 (0.095 g, 0.08 mmol) in THF (30 mL). The mixture was refluxed for 40 h, cooled to 0° C., quenched with water and extracted with Et2O. The organic layer was concentrated and the residue was purified over a silica gel column eluting with EtOAc/hexane (1:5) to give N-protected 6-methyl-7-azaindole (0.495 g, 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07456289B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-e565e8d0101240769f247e2833515134 |
| Source note | uspto-grants-2008_11 |