Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 609712Generated: October 30, 2026

Antimony pentachloride → HCID 22615656, compound

https://huagongshe.com/reaction/609712

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 numberUS05998412
Source datasetuspto-grants-1999_12
ORD IDord-31d98f1d37a24c7db80073463bdd98f8
Source noteuspto-grants-1999_12