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HRID 1420105作成日:2026年10月23日

2-Amino-4-methylpyridine → 2-(4-Methylpyridin-2-yl)-3-oxo-3h-benzo[d]isothiazole

https://huagongshe.com/ja/reaction/1420105

反応式

関与物質

役割名称HCID仕込み量
反応物2-Amino-4-methylpyridineHCID 1533—
反応物2-(Chlorothio)-benzoyl chlorideHCID 10910715—
溶媒PyridineHCID 1049—
生成物2-(4-Methylpyridin-2-yl)-3-oxo-3h-benzo[d]isothiazoleHCID 1587132737.1%

反応条件

温度50 °C

反応手順

Using the method of Fischer and Hurni (Arzneimittel Forsch., 1964;14:1301) 5.4 g (0.05 mol) of 2-amino-4-methylpyridine in 50 mL of pyridine at 10° C. was reacted with 10.3 g (0.05 mol) of 2-chlorosulfenylbenzoyl chloride. The mixture was heated to 50° C. and maintained at that temperature for 2 hours. The mixture was cooled to 25° C. and filtered. The solid was recrystallized from benzene to give 4.5 g of the title compound, mp 195°-196.5° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05889034
出典データセットuspto-grants-1999_03
ORD IDord-ef5ee94c30244c50bb1409a88010faa5
出典メモuspto-grants-1999_03