HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 58086725, compound → HCID 58087284, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 58086725 | HCID 58086725 | — |
| Reactant | HCID 58086855 | HCID 58086855 | — |
| Product | HCID 58087284 | HCID 58087284 | — |
Reaction Steps
The product of Step 2 of Scheme 41 can alternatively be reacted to form the corresponding compounds with methylene linker at the 3 position of the azaindole. For example, 4-(5-pyridin-3-yl 1H-pyrrolo[2,3-b]pyridin-3-ylmethyl)-indole-1-carboxylic acid butylamide P-1656 was prepared from 4-[Hydroxy-(5-pyridin-3-yl-1H-pyrrolo[2,3-b]pyridin-3-yl)-methyl]-indole-1-carboxylic acid butylamide 520 as shown in Scheme 41a.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143271B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-d9cc364b39364a8abb7ede5705313302 |
| Source note | uspto-grants-2012_03 |