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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 6217생성일: 2026년 10월 24일

Tetrahydrofuran → Pyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinol

https://huagongshe.com/ko/reaction/6217

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물BromocyclopropaneHCID 78037—
반응물MagnesiumHCID 5462224—
반응물5,6-dihydro-5-methyl-6-oxo-4H-imidazo [1,5-a]-pyrido [3,4-f][1,4]-diazepine-3-carboxaldehydeHCID 53687171—
반응물HCID 178418630HCID 178418630—
용매HexamethylphosphoramideHCID 12679—
생성물Pyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinolHCID 137226500—

반응 단계

To a solution of cyclopropyl magnesium bromide in dry tetrahydrofuran (prepared from 72 mg (3 mmole)) of magnesium and 362 mg (3 mmole) of cyclopropyl bromide in 4 ml of tetrahydrofuran was added at room temperature in one portion a suspension of 240 mg (1 mmole)of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo [1,5-a]-pyrido [3,4-f][1,4]-diazepine-3-carboxaldehyde suspended in a mixture of 1 ml of tetrahydrofuran and 1 ml of hexamethyl-phosphoramide. After 1 hour, the reaction was quenched with aqueous ammonium chloride and extracted with dichloromethane. Column chromatography (SiO2 -5% methanol in dichloromethane) yielded 120 mg of 5,6-dihydro-5-methyl-6-oxo-4H-imidazo-1,5-a]-pyrido-[3,4-f][1,4]-diazepin-3-yl cyclopropyl carbinol as an oil, (43%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05247079
출처 데이터셋uspto-grants-1993_09
ORD IDord-5d6c2380db7048b1ba438d1bba8589f6
출처 메모uspto-grants-1993_09