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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1944061생성일: 2026년 10월 27일

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

https://huagongshe.com/reaction/1944061

반응식

참여 물질

역할이름HCID투입량
반응물Methyl iodideHCID 6328—
반응물Carbon DisulfideHCID 6348—
반응물Sodium hydrideHCID 24758—
반응물Ethyl 2-(2-chloropyridin-3-yl)acetateHCID 15326671—
용매Dimethyl SulfoxideHCID 679—
생성물2-Methylsulfanylthieno[2,3-b]pyridine-3-carboxylic Acid Ethyl EsterHCID 1532667378.5%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08394822B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-94b5d704ac5343748d7bc7f10cb9533a
출처 메모uspto-grants-2013_03