HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613491Generated: November 1, 2026
Benzenesulfonyl chloride → HCID 178472453, compound
https://huagongshe.com/reaction/1613491
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178472452 | HCID 178472452 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178472453 | HCID 178472453 | 74% |
Reaction Steps
2-Amino-3-{1-[(cis-4-ethoxycarbonyl-cyclohexyl)carbamoyl]-cyclopentyl}propanoic acid t-butyl ester (0.605 g, 1.48 mmole) was dissolved in dry dichloromethane (25 ml) and treated at 0° C. with triethylamine (0.45 g, 4.4 mmole) and benzene sulphonyl chloride (0.24 ml, 1.84 mmole). After stirring for 16 hours at room temperature under nitrogen the dichloromethane was removed under vacuum, the residue taken up in diethyl ether (25 ml), washed with dilute hydrochloric acid, dilute sodium hydrogen carbonate and water, dried (Na2SO4) and the solvent evaporated under vacuum to give the crude product. Purification by column chromatography on silica, eluting with diethyl etherdichloromethane mixtures, gave pure title compound as a white foam (0.60 g, 74%). Found: C,61.38; H,7.85; N,5.06. C28H42N2O7S requires C,61.06; H,7.69; N,5.09%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05192800 |
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| Source dataset | uspto-grants-1993_03 |
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| ORD ID | ord-cd56313061f840d891626cee359576ed |
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| Source note | uspto-grants-1993_03 |
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