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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 67319생성일: 2026년 10월 24일

Formaldehyde → Ro 14-7437

https://huagongshe.com/ko/reaction/67319

반응식

참여 물질

역할이름HCID투입량
반응물FormaldehydeHCID 712—
반응물ethyl alpha-amino-1,3,4,5-tetrahydro-4-methyl-5-oxo-2H-1,4-benzodiazepin-2-ylidene-acetateHCID 70541641—
용매DichloromethaneHCID 6344—
생성물Ro 14-7437HCID 127597—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04346030
출처 데이터셋uspto-grants-1982_08
ORD IDord-34ed473f514a4ad88b0777a86c397cc9
출처 메모uspto-grants-1982_08