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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1515848Generated: November 4, 2026

5-nitro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine → 1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-amine

https://huagongshe.com/reaction/1515848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-nitro-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridineHCID 49758909—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-5-amineHCID 67229164100%

Reaction Steps

To a solution of 1-benzenesulfonyl-5-nitro-1H-pyrrolo[2,3-b]pyridine (2.8 g, 9.24 mmol) in tetrahydrofuran (50 mL) was added 10% palladium on activated carbon (0.98 g). The resulting mixture was stirred under hydrogen (50 psi) for 48 h at room temperature. The catalyst was removed by filtration and the filtrate was concentrated to afford 1-benzenesulfonyl-1H-pyrrolo[2,3-b]pyridin-5-ylamine (2.52 g, 100%) as a yellow oil which was used in the next step without purification: LC/MS m/e calcd for C13H11N3O2S [M+H]+ 274.32, observed 274.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222416B2
Source datasetuspto-grants-2012_07
ORD IDord-fb3fb45e7ec14b96bccb1431028ecdfb
Source noteuspto-grants-2012_07