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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1896472Generated: October 30, 2026

Bromide ion → HCID 15979795, compound

https://huagongshe.com/reaction/1896472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
Reactant4-Bromo-1-(triisopropylsilyl)-7-azaindoleHCID 11473655—
ReactantHCID 15979795HCID 15979795—
ReactantHCID 49758886HCID 49758886—
ReactantHCID 53629210HCID 53629210—
ProductHCID 15979795HCID 15979795—
Product4-Bromo-1H-pyrrolo[2,3-b]pyridineHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08518943B2
Source datasetuspto-grants-2013_08
ORD IDord-d344c27624b54513aa413ea57cc9cd42
Source noteuspto-grants-2013_08