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HRID 1944061作成日:2026年10月27日

Methyl iodide → 2-Methylsulfanylthieno[2,3-b]pyridine-3-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/1944061

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Carbon DisulfideHCID 6348—
反応物Sodium hydrideHCID 24758—
反応物Ethyl 2-(2-chloropyridin-3-yl)acetateHCID 15326671—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-Methylsulfanylthieno[2,3-b]pyridine-3-carboxylic Acid Ethyl EsterHCID 1532667378.5%

反応手順

To a solution of ethyl (2-chloropyridin-3-yl)acetate (D. H. Bremner et al., Synthesis, 1997, 949) (8.0 g, 40.0 mmol) and carbon disulfide (3.18 g, 42.0 mmol) in DMSO (100 mL) was added sodium hydride portionwise (2.4 g, 60.0 mmol). After 60 minutes stirring at room temperature the mixture was heated at 80° C. for 2 hours. After this time the reaction mixture was allowed to cool to room temperature and methyl iodide (7.6 g, 54.0 mmol) added. After 18 hours ice (50 mL) was added and a yellow precipitate formed which was isolated via filtration to give the title compound as a grey solid (7.95 g, 78%). δH (DMSO-d6) 8.60 (1H, dd, J 1.6, 8.2 Hz), 8.46, (1H, dd, J 1.6, 4.6 Hz), 7.35 (1H, dd, J 4.6, 8.2 Hz), 4.48 (2H, q, J=7.1 Hz), 2.71, (3H, s), 1.49 (3H, t, J=7.1 Hz).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08394822B2
出典データセットuspto-grants-2013_03
ORD IDord-94b5d704ac5343748d7bc7f10cb9533a
出典メモuspto-grants-2013_03