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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348542Generated: October 30, 2026

4-Methoxybenzenesulfonyl chloride → HCID 86594082, compound

https://huagongshe.com/reaction/348542

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Methoxybenzenesulfonyl chlorideHCID 7401—
ReactantHCID 86594083HCID 86594083—
ProductHCID 86594082HCID 86594082—

Reaction Steps

The title compound, MS (ISP): m/e=555.3 (M+H+), was prepared as for example 99, steps (A) to (F). Step (B) was performed using 4-chloro-aniline, and yielded (+/−)-trans-2-[4-(4-chloro-phenylamino)-piperidin-1-yl]-cyclohexanol, which was oxidized to (+/−)-2-[4-(4-chloro-phenylamino)-piperidin-1-yl]-cyclohexanone in step (C). This was then reacted with 4-methoxy-benzensulfonyl chloride in step (D), yielding (+/−)-N-(4-chloro-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-0e4735de6b4f4e32ace30ebe380dc343
Source noteuspto-grants-2007_02