HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromide ion → HCID 15979795, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromide ion | HCID 259 | — |
| Reactant | 4-Bromo-1-(triisopropylsilyl)-7-azaindole | HCID 11473655 | — |
| Reactant | HCID 15979795 | HCID 15979795 | — |
| Reactant | HCID 49758886 | HCID 49758886 | — |
| Reactant | HCID 53629210 | HCID 53629210 | — |
| Product | HCID 15979795 | HCID 15979795 | — |
| Product | 4-Bromo-1H-pyrrolo[2,3-b]pyridine | HCID 22273643 | — |
Reaction Steps
Synthesis of 4-propyl-1-(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)pyrrolidin-2-one 240. The further transformation of bromide x258 into the target product 240 is carried out in complete accordance with the transformation of bromide b191-1 into product ucb-108891-1 as described in examples 79.2 to 79.4. The yields are similar for intermediates 4-bromo-1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine x259, 1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridine-4-carbaldehyde x260 and 4-propyl-1-{[1-(triisopropylsilyl)-1H-pyrrolo[2,3-b]pyridin-4-yl]methyl}pyrrolidin-2-one x261. As a result, 1.0 g (5.1 mmol) of 4-bromo-1H-pyrrolo[2,3-b]pyridine x258 affords 0.45 g of 4-propyl-1-(1H-pyrrolo[2,3-b]pyridin-4-ylmethyl)pyrrolidin-2-one 240.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518943B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-d344c27624b54513aa413ea57cc9cd42 |
| Source note | uspto-grants-2013_08 |