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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051877Generated: October 27, 2026

Ethanol → 4-(2-(3-Oxa-8-azabicyclo[3.2.1]octane-8-carbonyl)-4-(4-chlorophenyl)thiazol-5-yl)benzenesulfonamide

https://huagongshe.com/reaction/1051877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(Aminosulphonyl)benzeneboronic acidHCID 22391977—
Reactant3-Oxa-8-azabicyclo[3.2.1]octan-8-yl(5-bromo-4-(4-chlorophenyl)thiazol-2-yl)methanoneHCID 89813296—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
Product4-(2-(3-Oxa-8-azabicyclo[3.2.1]octane-8-carbonyl)-4-(4-chlorophenyl)thiazol-5-yl)benzenesulfonamideHCID 7173716356.3%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

To a solution of 3-oxa-8-azabicyclo[13.2.1]octan-8-yl(5-bromo-4-(4-chlorophenyl) thiazol-2-yl)methanone (Step 3 of compound 68, 0.12 g, 0.29 mmol) in a mixture of toluene:ethanol (2 ml: 6 ml) were added 4-aminosulfonylbenzene boronic acid (0.07 g, 0.35 mmol) and potassium carbonate (0.12 g, 0.87 mmol) at 25° C. in a tube, the nitrogen gas was bubbled through reaction mixture for 15 minutes. To the reaction mixture was added tetrakis(triphenylphosphine)palladium(0) (0.017 g, 0.015 mmol) under nitrogen and tube was sealed. The reaction mixture was heated at 90-95° C. for 18 hr with stirring. The progress of reaction was monitored by TLC. The reaction mixture was cooled to 25° C. and filtered through celite. The residue was washed with ethanol (2×20 ml). The filtrate was concentrated under reduced pressure to obtain a crude product; which was purified by column chromatography over silica gel (100-200 mesh) using 40% ethyl acetate in hexanes as an eluent to obtain the title compound (0.08 g, 56.3%). MS: m/z 490 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-f24fe8d1d7d04659a1e099b16ea5ebe0
Source noteuspto-grants-2016_07