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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051896Generated: November 2, 2026

4-Bromobenzenesulfonamide → HCID 71736376, compound

https://huagongshe.com/reaction/1051896

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzenesulfonamideHCID 69696—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 89813354HCID 89813354—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylacetamideHCID 31374—
ProductHCID 71736376HCID 7173637632.7%

Reaction Conditions

Temperature150 °C

Reaction Steps

To a solution of 1-(4-(4-chlorophenyl)thiazol-2-yl)piperidin-2-one (Step 2 of compound 10, 0.5 g. 1.71 mmol) in dimethyl acetamide (5 ml) were added 4-bromobenzenesulfonamide (0.48 g, 2.05 mmol) and potassium acetate (0.42 g, 4.27 mmol) at 25° C. in a tube, the nitrogen gas was bubbled through reaction mixture for 15 minutes. To this was added palladium(II) acetate (0.02 g, 0.08 mmol) under nitrogen and the tube was sealed. The reaction mixture was heated at 150° C. for 15 hr under stirring. The progress of reaction was monitored by TLC. The reaction mixture was cooled to 25° C. and concentrated under reduced pressure. The residue was dissolved in ethyl acetate (30 ml), reaction mixture was washed with water (2×10 ml), dried over sodium sulphate and concentrated under reduced pressure to obtain a crude product; which was purified by preparative HPLC to obtain the title compound (0.25 g, 32.7%). MS: m/z 450 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-b29e80b86d6e4c0ba9a76d15a52af25a
Source noteuspto-grants-2016_07