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HRID 882021作成日:2026年10月24日

Acetic Anhydride → 4-((5-Fluoropyridin-2-yl)methoxy)pyridin-2(1H)-one

https://huagongshe.com/ja/reaction/882021

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AnhydrideHCID 7918—
反応物4-((5-Fluoropyridin-2-yl)methoxy)pyridine 1-oxideHCID 58092263—
生成物4-((5-Fluoropyridin-2-yl)methoxy)pyridin-2(1H)-oneHCID 5795034173%

反応条件

温度80 °C

反応手順

4-((5-Fluoropyridin-2-yl)methoxy)pyridine 1-oxide (1.76 g, 7.99 mmol) was heated to 140° C. in acetic anhydride (80 mL) for 5 h. The mixture was concentrated and then heated at 80° C. for 1 h in a mixture of MeOH (20 mL) and aqueous 1 N NaOH (15 mL). The resulting black solution was concentrated to a volume of 15 mL, and the solid was filtered off, rinsed with CH2Cl2 and dried under vacuum to provide the title compound (1.29 g, 73%) as a yellow solid: 1H NMR (500 MHz, DMSO-d6) δ 11.12 (s, 1H), 8.59 (d, J=2.9 Hz, 1H), 7.79 (ddd, J=8.7, 8.7, 2.9 Hz, 1H), 7.60 (dd, J=8.7, 4.5 Hz, 1H), 7.26 (d, J=7.3 Hz, 1H), 5.95 (dd, J=7.4, 2.6 Hz, 1H), 5.78 (d, J=2.5 Hz, 1H), 5.12 (s, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08993765B2
出典データセットuspto-grants-2015_03
ORD IDord-06a02b8338c3446395b158e4b8143ca7
出典メモuspto-grants-2015_03