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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 38814Generated: October 30, 2026

Benzenesulfonyl chloride → 6-Bromo-1-(phenylsulfonyl)-1H-indazole-4-carbonitrile

https://huagongshe.com/reaction/38814

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantSodium hydrideHCID 24758—
Reactant6-Bromo-1H-indazole-4-carbonitrileHCID 24728918—
SolventDimethylformamideHCID 6228—
Product6-Bromo-1-(phenylsulfonyl)-1H-indazole-4-carbonitrileHCID 6669215697.3%

Reaction Conditions

Temperature20 °C

Reaction Steps

To a solution of 6-bromo-1H-indazole-4-carbonitrile (5 g, 22.52 mmol) in N,N-dimethylformamide (50 ml) was added, in portions, sodium hydride (1.351 g, 33.8 mmol) and the mixture stirred at 20° C. for 15 mins then cooled to 0° C. when benzenesulfonyl chloride (3.16 ml, 24.77 mmol) was added dropwise. The mixture was stirred at 20° C. for 18 h then concentrated in vacuo and the residue partitioned between water (100 ml) and dichloromethane (100 ml). The organic layer was separated by hydrophobic frit and evaporated in vacuo to give the title compound as a yellow solid (7.94 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08524751B2
Source datasetuspto-grants-2013_09
ORD IDord-0a9c05e5ef1e43e8ac235bb79c926a4b
Source noteuspto-grants-2013_09