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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244706Generated: October 30, 2026

4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-B]pyridine → 1-(Phenylsulfonyl)-6-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl]-1H-indazol-4-amine

https://huagongshe.com/reaction/244706

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-B]pyridineHCID 45074561—
Reactant1-(phenylsulfonyl)-6-(trimethylstannanyl)-1H-indazol-4-amineHCID 58255743—
CatalystHCID 178418397HCID 178418397—
SolventDimethylformamideHCID 6228—
Product1-(Phenylsulfonyl)-6-[1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridin-4-yl]-1H-indazol-4-amineHCID 6702917127.3%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-Bromo-1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine (1.546 g, 4.59 mmol), 1-(phenylsulfonyl)-6-(trimethylstannanyl)-1H-indazol-4-amine (2 g, 4.59 mmol) and Pd(Ph3P)4 (0.265 g, 0.229 mmol) were added to N,N-dimethylformamide (30 mL) under nitrogen. The mixture was heated at 100° C. for 2 days then cooled at room temperature and concentrated in vacuo. The mixture was purified by column chromatography on silica (70 g) eluting with ammonia and methanol in DCM, then again using the Companion and eluting with a gradient of 30 to 85% MeCN (+0.1% TFA)/H2O (0.1% TFA). Fractions containing desired product were combined and the solvent was removed to afford the title compound as a brown solid (663 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658635B2
Source datasetuspto-grants-2014_02
ORD IDord-aea8e50aacea40f5b3f842f58e068114
Source noteuspto-grants-2014_02