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HRID 1378346作成日:2026年10月25日

2-Iodobenzene-1-sulfonyl chloride → N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-iodobenzenesulphonamide

https://huagongshe.com/reaction/1378346

反応式

関与物質

役割名称HCID仕込み量
反応物2-Iodobenzene-1-sulfonyl chlorideHCID 627400—
反応物3-Methoxy-5-methyl-2-pyrazinamineHCID 10701894—
溶媒PyridineHCID 1049—
生成物N-(3-Methoxy-5-methyl-2-pyrazinyl)-2-iodobenzenesulphonamideHCID 1017304744.4%

反応条件

温度70 °C

反応手順

2-IodobenzenesulphonyI chloride (obtained as described in J Org Chem, (1977), 42, 3265) (12.1 g) was added to a solution of 2-amino-3-methoxy-5-methylpyrazine (5.6 g) in pyridine (100 ml) and the solution was heated at 70° C. for 8 hours. Volatile material was removed by evaporation and water (200 ml) was added to the residue. The mixture was extracted with ethyl acetate (2×200 ml) and the extracts were washed with 2M hydrochloric acid (200 ml) and water (200 ml). The extracts were dried (MgSO4) and the solvent was removed by evaporation. The residue was triturated with ether to give 2-iodo- N-(3-methoxy-5-methylpyrazin-2-yl)benzenesulphonamide (7.2 g), m.p. 136°-138° C.; 1H NMR (d6 -DMSO): 2.3 (s, 3H), 3.9 (s, 3H), 7.3(dt, 1H), 7.5-7.65 (m, 2H), 8.05-8.15 (m, 2H), 10.7-10.8 (br s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05668137
出典データセットuspto-grants-1997_09
ORD IDord-6f394b1814db46aaa587b379fd15cb43
出典メモuspto-grants-1997_09