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HRID 2308466作成日:2026年10月25日

Pyridine → 5-Methyl-thiophene-2-carboxylic acid (7-bromo-4-methoxybenzothiazol-2-yl)-amide

https://huagongshe.com/reaction/2308466

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物5-Methylthiophene-2-carbonyl chlorideHCID 2760083—
反応物7-Bromo-4-methoxy-1,3-benzothiazol-2-amineHCID 22283200—
溶媒DichloromethaneHCID 6344—
生成物5-Methyl-thiophene-2-carboxylic acid (7-bromo-4-methoxybenzothiazol-2-yl)-amideHCID 86584910—

反応手順

2-Amino-7-bromo-4-methoxybenzothiazol (2.33 g, 9 mmol) is dissolved in dichloromethane (100 ml) and at 0° C. treated with pyridine (2.2 ml, 27 mmol) and 5-methyl-thiophene-2-carbonyl chloride (2.2 g, 13.5 mmol). The reaction mixture is allowed to warm to room temperature and after stirring for additional 18 h quenched with water (100 ml). After separation of the phases, the aqueous phases are extracted twice with ethyl acetate. The combined organic layers are then washed with brine, dried and avaporated to dryness. Flash chromatography on silica (eluent ethyl acetate/cyclohexane 1:1 to 4:1) and final recrystallization from ethyl acetate affords the product as off-white solid. (34 mg, 69%). MS: m/e=384 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06835732B2
出典データセットuspto-grants-2004_12
ORD IDord-8b65a03d0e7840c781f37db88e0ef02b
出典メモuspto-grants-2004_12