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HRID 710581作成日:2026年10月24日

Pyridine → 3-Bromo-7-(ethylamino)-1-methyl-1,6-naphthyridin-2(1H)-one

https://huagongshe.com/ja/reaction/710581

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物BromoselenobenzeneHCID 123446—
反応物7-(Ethylamino)-1-methyl-1,6-naphthyridin-2(1H)-oneHCID 67378368—
溶媒DichloromethaneHCID 6344—
生成物3-Bromo-7-(ethylamino)-1-methyl-1,6-naphthyridin-2(1H)-oneHCID 67378359—

反応条件

温度39 °C

反応手順

To a solution of 7-(ethylamino)-1-methyl-1,6-naphthyridin-2(1H)-one (20 mg, 0.1 mmol) and pyridine (27 μL, 0.3 mmol) in DCM (2 mL) was added phenylselenium bromide (72 mg, 0.3 mmol). The mixture was heated at 39° C. for 6 h, and then the solvent was removed under vacuum. The residue was chromatographed on silica gel (30% ethyl acetate in hexanes eluant) to provide the title compound. MS (m/z) 282.0 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09181238B2
出典データセットuspto-grants-2015_11
ORD IDord-812fa3d5a0cb45b989bb734a57ddfeb3
出典メモuspto-grants-2015_11