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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 217959Generated: October 30, 2026

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

https://huagongshe.com/reaction/217959

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-Pyrrolo(2,3-b)pyridineHCID 9222—
ReactantDiisopropylcarbodiimideHCID 12734—
ReactantDiisopropylethylamineHCID 81531—
Reactant1H-Pyrrolo[2,3-b]pyridine-3-carboxylic acid, 1-(1,1-dimethylethyl)-5-nitro-HCID 66924396—
Solventdichloromethane N,N-dimethylformamideHCID 22350042—
Product1H-IndazoleHCID 9221—

Reaction Steps

To the AMEBA II resin (0.1 g, 1 mmol/g, 0.1 mmol) in DCM/DMF (1:1, 2 ml), 1-tert-butyl-5-nitro-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid (3 eq), DIC (1.5 eq) DMAP (0.5 eq) and DIPEA (1 eq) were added. The reaction mixture was shaken at room temperature for 20 hours and then the resin was isolated by filtration. The resin was washed sequentially with DMF (2 ml), DCM (2 ml), DMF (2 ml), DCM (2 ml), MeOH (2 ml), DCM (2 ml), MeOH (2 ml), DCM (2 ml), MeOH (2 ml), DCM (2 ml) and dried in vacuo to give the resin bound 7-azaindole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08198298B2
Source datasetuspto-grants-2012_06
ORD IDord-985801bdca9e4e6e9c6ea0c17f7e1139
Source noteuspto-grants-2012_06