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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348544Generated: October 31, 2026

4-Methoxybenzenesulfonyl chloride → HCID 86594084, compound

https://huagongshe.com/reaction/348544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantHCID 86594085HCID 86594085—
ProductHCID 86594084HCID 86594084—

Reaction Steps

The title compound, MS (ISP): m/e=589.4 (M+H+), was prepared as for example 99, steps (A) to (F). Step (B) was performed using 4-trifluoromethyl-aniline, and yielded (+/−)-trans-2-[4-(4-trifluoromethyl-phenylamino)-piperidin-1-yl]-cyclohexanol, which was oxidized to (+/−)-2-[4-(4-trifluoromethyl-phenylamino)-piperidin-1-yl]-cyclohexanone in step (C). This was then reacted with 4-methoxy-benzensulfonyl chloride in step (D), yielding (+/−)-N-(4-trifluoromethyl-phenyl)-4-methoxy-N-[1-(2-oxo-cyclohexyl)-piperidin-4-yl]-benzenesulfonamide. The final step (F) was performed with bromobenzene.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176316B2
Source datasetuspto-grants-2007_02
ORD IDord-5c6f67a06c5246989f7eda4bb13d26c4
Source noteuspto-grants-2007_02