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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-Bromo-1H-indazole-4-carbonitrile | HCID 24728918 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-1-(phenylsulfonyl)-1H-indazole-4-carbonitrile | HCID 66692156 | 97.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08524751B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-0a9c05e5ef1e43e8ac235bb79c926a4b |
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| Source note | uspto-grants-2013_09 |
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