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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2068026Generated: November 1, 2026

1H-Pyrrolo(2,3-b)pyridine → 1H,2H,3H-pyrrolo(2,3-b)pyridine

https://huagongshe.com/reaction/2068026

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantHCID 178418361HCID 178418361—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product1H,2H,3H-pyrrolo(2,3-b)pyridineHCID 1001188979%

Reaction Steps

A solution of 7-azaindole (20.0 g, 169 mmol) in ethanol (200 ml) was treated with wet Raney Nickel (4 g, 50% water) and stirred in a hydrogen atmosphere at 5 atmospheres pressure at 95° C. over 2 days. The reaction mixture was filtered through diatomaceous earth and the filtrate evaporated under vacuum The residue was purified by column chromatography eluting with ethyl acetate followed by increasingly polar mixtures of methylene chloride and methanol (saturated with ammonia) to give 7-azaindoline (12.1 g, 79%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293902B2
Source datasetuspto-grants-2012_10
ORD IDord-4bd497eaa983440db7cb9c66db3068fa
Source noteuspto-grants-2012_10