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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1856901Generated: October 29, 2026

Antimony pentachloride → HCID 22615656, compound

https://huagongshe.com/reaction/1856901

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAntimony pentachlorideHCID 24294—
ReactantSulfuryl chlorideHCID 24648—
ReactantMethyl 1-aminocyclohexane-1-carboxylate hydrochlorideHCID 22645079—
SolventAcetonitrileHCID 6342—
ProductHCID 22615656HCID 2261565685%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06143744
Source datasetuspto-grants-2000_11
ORD IDord-41260f07bc5c4e3da48e2b6cea834dd3
Source noteuspto-grants-2000_11