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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048545Generated: October 31, 2026

Cyclobutanesulfonamide → HCID 67999193, compound

https://huagongshe.com/reaction/1048545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclobutanesulfonamideHCID 15238957—
Reactant(3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-hydroxybutan-2-yl)-3-methylpiperidin-2-oneHCID 58573282—
ProductHCID 67999193HCID 67999193—

Reaction Conditions

Temperature40 °C

Reaction Steps

The title compound was prepared from (3S,5R,6S)-3-allyl-5-(3-chlorophenyl)-6-(4-chlorophenyl)-1-((S)-1-hydroxybutan-2-yl)-3-methylpiperidin-2-one (Example 91, Step B, 250 mg, 0.560 mmol) and cyclobutanesulfonamide (Example 271G, 256 mg, 1.894 mmol) using the general procedure described in Step A of Example 272, albeit with an oil bath heated at 40° C. The crude product was purified by silica gel chromatography eluting with a gradient of EtOAc in hexanes. The product was obtained as a white powder (220 mg, 70%). LCMS (ESI): m/z=563.2 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08569341B2
Source datasetuspto-grants-2013_10
ORD IDord-e8498276ccff4d8a8b6a2147343d4d41
Source noteuspto-grants-2013_10