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HRID 500668作成日:2026年10月26日

4-Methoxybenzohydrazide → Ethyl 6-{2-[2-(4-methoxybenzoyl)hydrazino]-2-oxoethyl}-1-benzothiophene-2-carboxylate

https://huagongshe.com/reaction/500668

反応式

関与物質

役割名称HCID仕込み量
反応物4-MethoxybenzohydrazideHCID 76792—
反応物3-(Ethyliminomethylideneamino)propyl-dimethylazanium chlorideHCID 5351932—
反応物[2-(Ethoxycarbonyl)-1-benzothien-6-yl]acetic acidHCID 59424238—
溶媒DimethylformamideHCID 6228—
生成物Ethyl 6-{2-[2-(4-methoxybenzoyl)hydrazino]-2-oxoethyl}-1-benzothiophene-2-carboxylateHCID 5942423749.8%

反応手順

To a solution of [2-(ethoxycarbonyl)-1-benzothien-6-yl]acetic acid (100 mg, 0.38 mmol) and 4-methoxybenzohydrazide (63 mg, 0.38 mmol) in 2 mL DMF was added 3-{[(ethylimino)methylene]amino}-N,N-dimethylpropane-1-aminium chloride (91 mg, 0.47 mmol). The reaction was stirred at ambient temperature for 12 hours. The reaction mixture was loaded directly onto a reverse phase C18 column for purification to give 78 mg (49%) of the title compound as a white solid. LC/MS (EI): cal'd 413.1 (MH+), exp 413.1 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07772238B2
出典データセットuspto-grants-2010_08
ORD IDord-615a74f836c34a0680e557166989e297
出典メモuspto-grants-2010_08