HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856901Generated: October 29, 2026
Antimony pentachloride → HCID 22615656, compound
https://huagongshe.com/reaction/1856901
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Antimony pentachloride | HCID 24294 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Methyl 1-aminocyclohexane-1-carboxylate hydrochloride | HCID 22645079 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 22615656 | HCID 22615656 | 85% |
Reaction Steps
To a suspension of methyl 1-aminocyclohexane-1-carboxylate HCl salt (4.06 g, 20.9 mmol) in acetonitrile (37 ml) was added sulfuryl chloride (26.2 ml, 326 mmol) and antimony pentachloride (0.17 ml, 2.4 mmol). The reaction was heated at 80° C. using a calcium sulfate drying tube overnight. The reaction was concentrated in vacuo to give methyl 1-(chlorosulfonylamino)cyclohexane-1-carboxylate (85%) as a yellow oil that was used without further purification. This material was converted to N-hydroxy-1-{[4-(4-chlorophenyl)-piperazine-1-sulfonyl]amino}cyclohexane-1-carboxamide by following Examples 2 and Example 13 except that the reaction was heated at 45° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06143744 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-41260f07bc5c4e3da48e2b6cea834dd3 |
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| Source note | uspto-grants-2000_11 |
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