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HRID 48338作成日:2026年10月24日

3,4-Dichlorobenzaldehyde → (E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-(3-thienyl)-1H-1,4-benzodiazepine dihydrochloride

https://huagongshe.com/ja/reaction/48338

反応式

関与物質

役割名称HCID仕込み量
反応物3,4-DichlorobenzaldehydeHCID 22710—
反応物Sodium hydrideHCID 24758—
反応物(1-Methyl-8-thiophen-3-yl-1,2,3,4-tetrahydrobenzo [e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl esterHCID 86585816—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-(3-thienyl)-1H-1,4-benzodiazepine dihydrochlorideHCID 69893578165.2%

反応手順

To 105 mg (0.27 mmol) of (1-methyl-8-thiophen-3-yl-1,2,3,4-tetrahydrobenzo[e][1,4]diazepin-5-ylidenemethyl)phosphonic acid diethyl ester in 2 ml of tetrahydrofuran was added 19 mg (0.47 mmol) of sodium hydride (60% dispersion in mineral oil). After 10 minutes 49 mg (0.28 mmol) of 3,4-dichlorobenzaldehyde was added and the mixture was stirred for 3 hours. The product was purified by column chromatography (20 g IST pre-packed column) eluting with 1% methanol/dichloromethane and treated with 0.15 ml of 4M hydrogen chloride in dioxan. The solvent was evaporated and the residue was recrystallized from acetone to give 75 mg of (E)-5-(3,4-dichlorostyryl)-2,3-dihydro-1-methyl-8-(3-thienyl)-1H-1,4-benzodiazepine dihydrochloride as an orange solid; MS: 412 (M+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06703387B2
出典データセットuspto-grants-2004_03
ORD IDord-e6b4d448a4774602ba6420691c38eed0
出典メモuspto-grants-2004_03