HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 7027Generated: October 26, 2026
4-Chlorobenzenesulfonyl chloride → cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide
https://huagongshe.com/reaction/7027
Participants
| Role | Name | HCID | Charge |
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| Reactant | 4-Chlorobenzenesulfonyl chloride | HCID 7398 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | cis-2-Aminocyclohexanecarboxamide | HCID 2724813 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | cis-2-(4-Chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide | HCID 69655699 | 45.1% |
Reaction Steps
To a solution of cis-2-aminocyclohexanecarboxylic acid amide (2.0 g, 14.0 mmol), and triethylamine (3.9 mL, 28 mmol) in dichloromethane (100 mL) was added 4-chlorobenzenesulfonyl chloride (2.95 g, 14.0 mmol). The resulting solution was stirred at room temperature for 18 h. The reaction was then diluted with dichloromethane (200 mL) and washed with H2O, 1.0 M HCl, brine, and dried over Na2SO4. Further purification by flash chromatography (silica gel, 1% to 10% MeOH/CHCl3) afforded cis-2-(4-chlorobenzenesulfonylamino)-cyclohexanecarboxylic acid amide (2.0 g) as a white solid in 45% yield over three steps: 1H NMR (DMSO-d6) δ 7.82 (m, 2 H), 7.63 (m, 2 H), 7.56 (d, 1 H, J=7.0 Hz), 7.22 (s br, 1 H), 6.80 (s br, 1 H), 3.43 (m, 1 H), 2.37 (m,1 H), 1.72 (m, 2 H), 1.45 (m, 3 H), 1.15 (m, 3 H); MS m/e 317.05 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07084178B2 |
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| Source dataset | uspto-grants-2006_08 |
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| ORD ID | ord-5401af972bfd4b98b671d0bcf01afd38 |
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| Source note | uspto-grants-2006_08 |
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