HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 631877Generated: October 25, 2026
Benzenesulfonyl chloride → N-(2-Cyano-3-cyclopropylphenyl)-benzenesulfonamide
https://huagongshe.com/reaction/631877
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Amino-6-cyclopropylbenzonitrile | HCID 66747252 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(2-Cyano-3-cyclopropylphenyl)-benzenesulfonamide | HCID 68296410 | 39.4% |
Reaction Steps
Benzenesulfonyl chloride (0.093 g) was added to a solution of 2-amino-6-cyclopropyl-benzonitrile (Intermediate 10, 0.07 g) in DCM (4 mL) and pyridine (0.1 mL). The mixture was stirred for 5 hours, then a further aliquot of benzenesulfonyl chloride (0.093 g) was added together with triethylamine (0.12 mL) and the mixture was stirred overnight. The reaction mixture was washed with water, and the organic solution was dried with magnesium sulfate, filtered and the filtrate was evaporated under vacuum. The residue was purified by flash chromatography on silica, eluting with a mixture of ethyl acetate and cyclohexane. The fractions containing the desired product were combined and evaporated to give the title compound as a colorless oil (0.052 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09321740B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-28c9045e40b843c8a60b74027cf27e2a |
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| Source note | uspto-grants-2016_04 |
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