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HRID 67319作成日:2026年10月25日

Formaldehyde → Ro 14-7437

https://huagongshe.com/reaction/67319

反応式

関与物質

役割名称HCID仕込み量
反応物FormaldehydeHCID 712—
反応物ethyl alpha-amino-1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetateHCID 70541641—
溶媒DichloromethaneHCID 6344—
生成物Ro 14-7437HCID 127597—

反応手順

1.0 g of ethyl α-amino-1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetate are dissolved in 20 ml of methylene chloride, treated with 0.65 ml of 37 percent aqueous formaldehyde solution and stirred in the presence of air at room temperature for 2 hours. The solution is subsequently washed twice with 10 ml of water each time. The organic phase is separated, dried and decolourised with active carbon. After filtration of the carbon, the filtrate is evaporated in vacuo and the residue is chromatographed on 20 g of silica gel. Elution is carried out firstly with chloroform and subsequently with chloroform/ethanol (985:15). The fractions which contain ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate as the main component are combined and evaporated in vacuo. The residue is dissolved in ethanol and crystallised by the addition of diisopropyl ether. There is obtained ethyl 5,6-dihydro-5-methyl-6-oxo-4H-imidazo[1,5-a][1,4]benzodiazepine-3-carboxylate of melting point 162°-164° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04346030
出典データセットuspto-grants-1982_08
ORD IDord-34ed473f514a4ad88b0777a86c397cc9
出典メモuspto-grants-1982_08