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HRID 33822作成日:2026年10月24日

Acetic Acid → 2-(Pyridin-4-yl)-1-(4-(quinolin-2-ylmethoxy)phenyl)ethan-1-one

https://huagongshe.com/ja/reaction/33822

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物4-MethylpyridineHCID 7963—
反応物Lithium diisopropylamideHCID 2724682—
反応物Benzamide, N-methoxy-N-methyl-4-(2-quinolinylmethoxy)-HCID 44234674—
溶媒TetrahydrofuranHCID 8028—
生成物2-(Pyridin-4-yl)-1-(4-(quinolin-2-ylmethoxy)phenyl)ethan-1-oneHCID 3367972780%

反応条件

温度-78 °C

反応手順

To a solution of Lithium diisopropyl amide (1.0M) in tetrahydrofuran was added 4-picoline dropwise (7.55 ml, 5 eq.) at 0° C. under N2. After 30 min the anion was cooled to −78° C. In a separate round bottom flask N-Methoxy-N-methyl-4-(quinolin-2-ylmethoxy)-benzamide (5.0, 15.5 mmole) was dissolved in tetrahydrofuran (77 ml, 0.2M) and cooled to −78° C. under N2. 1.2 eq. of the 4-picoline anion was added dropwise to the amide solution. After 45 min, 1 eq. more of the 4-picoline anion was added. After an addition 30 min, acetic acid (40 ml) was added dropwise and the reaction was slowly warmed to ambient temperature. The solid product (acetate salt) was filtered and partitioned between saturated sodium bicarbonate and dichloromethane. The layers were separated, dried magnesium sulfate filtered and concentrated to provide the title compound as a tan solid (4.41 g, 80%). 1H NMR (400 MHz, CDCl3) δ 8.52 (d, J=5.8 Hz, 2 H), 8.19 (d, J=8.7 Hz, 1 H), 8.07 (d, J=8.7 Hz, 1H), 7.93 (m, 2 H), 7.82 (d, J=8.3 Hz, 1 H), 7.75 (m, 1 H), 7.61 (d, J=8.3 Hz, 1 H), 7.54 (dt, J=7.9, 1.0 Hz, 1 H), 7.23 (m, 2 H) 7.07 (m, 2H), 5.42 (s, 2H), 4.19 (s, 2H); MS: (M+H m/z=355.2).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07429665B2
出典データセットuspto-grants-2008_09
ORD IDord-fa627596c921474d9295989408bf324f
出典メモuspto-grants-2008_09