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HRID 1774889作成日:2026年10月25日

Sodium Carbonate → Ethanesulfonic acid [5-(8-fluoro-1-methyl-2-oxo-1,2-dihydro-quinolin-6-yl)-pyridin-3-ylmethyl]-amide

https://huagongshe.com/reaction/1774889

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium CarbonateHCID 10340—
反応物HCID 58215658HCID 58215658—
反応物8-Fluoro-1-methyl-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-YL)-3,4-dihydroquinolin-2(1H)-oneHCID 72698826—
触媒HCID 178418476HCID 178418476—
溶媒DimethylformamideHCID 6228—
生成物Ethanesulfonic acid [5-(8-fluoro-1-methyl-2-oxo-1,2-dihydro-quinolin-6-yl)-pyridin-3-ylmethyl]-amideHCID 8667923910.1%

反応条件

温度120 °C

反応手順

A mixture of 8-fluoro-1-methyl-6-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-3,4-dihydro-1H-quinolin-2-one (example 208 [E], 20 mg, 0.066 mmol), ethanesulfonic acid (5-bromo-pyridin-3-ylmethyl)-amide (intermediate A-11, 27.4 mg, 0.098 mmol), bis(triphenylphosphine)-palladium(II) chloride (4.6 mg, 0.0066 mmol), and aq. sodium carbonate solution (2 N, 0.07 mL) in DMF (1 mL) was heated in a microwave at 120° C. for 30 minutes. After dilution of the reaction mixture with EtOAc, the organic layer was washed with water, dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was then purified by prep-HPLC to afford the title compound (2.5 mg, 10%) as a white solid. MS: 376.3 (M+H+)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09260408B2
出典データセットuspto-grants-2016_02
ORD IDord-555770becf1f4df7afc2c1e5a7b41b31
出典メモuspto-grants-2016_02