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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075814Generated: November 2, 2026

4-Bromobenzenesulfonamide → 2-Phenylbenzene-1-sulfonamide

https://huagongshe.com/reaction/2075814

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzenesulfonamideHCID 69696—
CatalystPalladiumHCID 23938—
Product2-Phenylbenzene-1-sulfonamideHCID 12371520—

Reaction Steps

In Scheme 1 the compounds of the invention, 1, are prepared in 4 steps. Sulfonylation of valine methyl ester with 4-Bromo-benzenesulfonyl chloride was carried out under Hunig base condition to give sulfonamide intermediate 1. This 4-Bromo-benzenesulfonamide was furthered coupled with boronate ester using Palladium catalyst under Suzuki coupling condition to provide biphenyl sulfonamide Intermediate 2. Biphenyl sulfonamide intermediate 2 was then alkylated with various alkylating reagents to provide biphenyl sulfonamide ester (Intermediate 3). Hydrolysis of intermediate 3 was carried out using bases such as NaOH, or LiOH to afford the final product 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07923446B2
Source datasetuspto-grants-2011_04
ORD IDord-810f69097ba34e78a15d70781b7cb2c2
Source noteuspto-grants-2011_04