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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1051892Generated: November 2, 2026

Ethanol → HCID 89813524, compound

https://huagongshe.com/reaction/1051892

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantPotassium CarbonateHCID 11430—
Reactant2,4-Difluorophenylboronic acidHCID 2734334—
Reactant2-(3-Azabicyclo[3.1.0]hexan-3-yl)-4-bromothiazoleHCID 89813337—
CatalystHCID 178418397HCID 178418397—
SolventTolueneHCID 1140—
ProductHCID 89813524HCID 8981352477.4%

Reaction Conditions

Temperature92.5 °C

Reaction Steps

To a solution of 2-(3-azabicyclo[3.1.0]hexan-3-yl)-4-bromothiazole (Step-1 of compound 66, 0.29 g, 1.16 mmol) in a mixture of toluene: ethanol (4 ml:16 ml) were added (2,4-difluorophenyl) boronic acid (0.20 g, 1.28 mmol) and potassium carbonate (0.32 g, 2.32 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) (0.067 g, 0.058 mmol) under nitrogen and the 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; residue was washed with ethyl acetate (2×10 ml). The filtrate was concentrated under reduced pressure to obtain a crude product; which was purified by flash column chromatography using 10% ethyl acetate in hexanes as an eluent to obtain the title compound (0.25 g, 77.0%). MS: m/z 279 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388196B2
Source datasetuspto-grants-2016_07
ORD IDord-091dd04808f44804bb9a3210181a8494
Source noteuspto-grants-2016_07