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HRID 2358864作成日:2026年10月27日

Hydrazine hydrate (1:1) → 3-Anilino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridine-2-carbohydrazide

https://huagongshe.com/reaction/2358864

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrazine hydrate (1:1)HCID 24654—
反応物Sodium BicarbonateHCID 516892—
反応物Ethyl 3-(phenylamino)-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridine-2-carboxylateHCID 9865198—
溶媒1-EthoxyethanolHCID 10129898—
生成物3-Anilino-6-oxo-7-phenyl-6,7-dihydrothieno[2,3-b]pyridine-2-carbohydrazideHCID 6845413546%

反応条件

温度120 °C

反応手順

To a stirred solution of Example 1 (200 mg, 0.5 mmol) in ethoxyethanol (5 mL) was added hydrazine hydrate (1.5 mmol). The reaction mixture was heated to 120° C. for 6 h. Upon cooling the reaction mixture was poured into sat NaHCO3 aq and extracted with DCM (×2). The combined organic fractions were dried (MgSO4) and concentrated in vacuo. Purification by flash column chromatography (silica, 5% EtOH in DCM) gave the title compound (86 mg, 46%). δH (CDCl3) 8.76 (1H, br s), 8.60 (1H, br s), 7.55-7.7 (3H, m), 7.4-7.5 (2H, m), 7.25-7.35 (3H, m), 6.9-7.0 (2H, m), 6.35 (1H, d, J 10 Hz), 4.3 (2H, br s). LCMS (ES+) RT 2.84 minutes, 377 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07763729B2
出典データセットuspto-grants-2010_07
ORD IDord-297f06aaec354215ad402a5e7adb2fab
出典メモuspto-grants-2010_07