Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 520507Generated: October 30, 2026

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

https://huagongshe.com/reaction/520507

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 numberUS09326987B2
Source datasetuspto-grants-2016_05
ORD IDord-9d5461560f704c6faf62a5b3dee37aa8
Source noteuspto-grants-2016_05