HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2110267Generated: November 1, 2026
3-Chlorobenzenesulphonyl chloride → HCID 57636438, compound
https://huagongshe.com/reaction/2110267
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-Chlorobenzenesulphonyl chloride | HCID 17909 | — |
| Reactant | HCID 39218501 | HCID 39218501 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 57636438 | HCID 57636438 | 59.5% |
Reaction Steps
To 3-chlorobenzenesulfonyl chloride (43.4 mg, 0.205 mmol) in 1.0 mL pyridine was added 3-(2-chloro-phenyl)-1H-indazol-6-ylamine (50.0 mg, 0.205 mmol). The solution was heated to 120° C. and stirred for one hour, then cooled and concentrated under reduced pressure. The residue was chromatographed through silica gel (hexanes/EtOAc 0-30%) to give 51.0 mg of 3-Chloro-N-[3-(2-chloro-phenyl)-1H-indazol-6-yl]-benzenesulfonamide, MP=187-189° C., MS (M+H)=419.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07517901B2 |
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| Source dataset | uspto-grants-2009_04 |
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| ORD ID | ord-866bb8e69c2148f48823186cab310d25 |
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| Source note | uspto-grants-2009_04 |
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