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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365481Generated: October 30, 2026

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

https://huagongshe.com/reaction/1365481

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 numberUS07888508B2
Source datasetuspto-grants-2011_02
ORD IDord-4b4fbf224302491292d9d6f843524723
Source noteuspto-grants-2011_02