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HRID 67368作成日:2026年10月24日

Ethyl Acetate → Ro 14-7437

https://huagongshe.com/ja/reaction/67368

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Dimethylformamide diethylacetalHCID 70913—
反応物ethyl alpha-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetateHCID 70542724—
生成物Ro 14-7437HCID 127597—

反応手順

4.1 g of ethyl α-amino-1,3,4,5-tetrahydro-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate are dissolved in 25 ml of ethyl acetate, treated with 3.1 ml (18.1 mmol) of N,N-dimethylformamide diethyl acetal and heated to boiling under reflux for 0.5 hour. After cooling, the separated material is filtered off under suction and recrystallised from ethanol. After chromatography of the mother liquor, there is obtained a second portion of ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of the same purity; melting point 166°-168° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346031
出典データセットuspto-grants-1982_08
ORD IDord-7179a83ad66b4a8b8fe1f5f7ae03e1f3
出典メモuspto-grants-1982_08