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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051899Generated: November 1, 2026

4-Bromobenzenesulfonamide → 4-(2-(3-Azabicyclo[3.1.0]hexan-3-ylmethyl)-4-(4-chlorophenyl)thiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1051899

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-BromobenzenesulfonamideHCID 69696—
ReactantPotassium AcetateHCID 517044—
ReactantHCID 89813117HCID 89813117—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylacetamideHCID 31374—
Product4-(2-(3-Azabicyclo[3.1.0]hexan-3-ylmethyl)-4-(4-chlorophenyl)thiazol-5-yl)benzenesulfonamideHCID 7173539822%

Reaction Conditions

Temperature150 °C

Reaction Steps

4-bromobenzenesulfonamide (0.37 g, 1.57 mmol) and potassium acetate (0.28 g, 2.87 mmol) were added to a solution of 2-(3-azabicyclo[3.1.0]hexan-3-ylmethyl)-4-(4-chlorophenyl)thiazole (Step-2 of compound 102, 0.42 g, 1.43 mmol) in a DMA (5 ml) in a tube at 25° C. Nitrogen gas was bubbled through the reaction mixture for 15 minutes. Palladium acetate (0.032 g, 0.14 mmol) was then added to the reaction mixture under nitrogen atmosphere and the tube was sealed. The reaction mixture was heated at 150° C. for 20 hrs under stirring. The progress of the reaction was monitored by TLC. The reaction mixture was then cooled to 25° C. and filtered through celite. The celite cake was washed with ethyl acetate (20 ml). The combined filtrate was concentrated under reduced pressure to obtain a crude product, which was then purified by column chromatography using 30% ethyl acetate in hexanes as an eluent to obtain the title compound (0.14 g, 21.4%). MS: m/z 446 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-53a1ef27cef4423db3f70cb0fc59f3a3
Source noteuspto-grants-2016_07