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HRID 339533作成日:2026年10月25日

Thionyl Chloride → 4-Iodo-3-nitro-N-[4-(6-methoxybenzothiazol-2-yl)-phenyl]-benzamide

https://huagongshe.com/reaction/339533

反応式

関与物質

役割名称HCID仕込み量
反応物Thionyl ChlorideHCID 24386—
反応物DiisopropylethylamineHCID 81531—
反応物4-(6-Methoxy-1,3-benzothiazol-2-yl)anilineHCID 391870—
反応物4-Iodo-3-nitrobenzoic acidHCID 11208598—
溶媒TetrahydrofuranHCID 8028—
生成物4-Iodo-3-nitro-N-[4-(6-methoxybenzothiazol-2-yl)-phenyl]-benzamideHCID 6731320578%

反応手順

A mixture of 4-iodo-3-nitrobenzoic acid (0.286 g, 0.976 mmol) and thionyl chloride (5 ml) was heated under reflux for 3 h. The reaction mixture was cooled to room temperature and the excess reagent and solvent was removed under reduced pressure to give the crude acid chloride. The amide was prepared as described in the Amide Coupling section using the crude acid chloride, 2-(4-aminophenyl)-6-methoxybenzothiazole (0.25 g, 0.976 mmol) and Hunig's base (0.151 g, 1.17 mmol) in dry THF (10 ml) to give the title compound (0.403 g, 78%) as a yellow solid after work-up.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08895313B2
出典データセットuspto-grants-2014_11
ORD IDord-84cb27c98a12420a880553ff01b43a91
出典メモuspto-grants-2014_11