HuagongsheHuagongshe Chemistry Print Report · For research reference only
1H-Indazole → 5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1H-Indazole | HCID 9221 | — |
| Reactant | Boronic Acid | HCID 61668 | — |
| Reactant | 5-bromo-1H-pyrrolo[2,3-b]pyridine | HCID 10307932 | — |
| Reactant | 5-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrolo(2,3-b)pyridine | HCID 24208789 | — |
| Product | 5-(Pyridin-3-yl)-1H-pyrrolo[2,3-b]pyridine | HCID 51358551 | — |
Reaction Steps
Additional compounds were prepared following the protocol of Scheme 32, either by substituting pyridine-3-boronic acid with an appropriate boronic acid or by substituting the 5-bromo-7-azaindole with 5-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrrolo[2,3-b]pyridine and reacting with a suitable aryl or heteroaryl halide (i.e. coupling with the boronic acid ester on the azaindole, and the halide on the group to be coupled to the 5-position of the azaindole). The following compounds were prepared by this procedure:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863288B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-d25de20224de4148b65b1e49bb297509 |
| Source note | uspto-grants-2011_01 |