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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53554생성일: 2026년 10월 26일

Benzaldehyde → 11-Cyclopropyl-5,11-dihydro-4-phenacyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one

https://huagongshe.com/reaction/53554

반응식

참여 물질

역할이름HCID투입량
반응물BenzaldehydeHCID 240—
반응물NevirapineHCID 4463—
반응물Sodium hydrideHCID 24758—
반응물Lithium diisopropylamideHCID 2724682—
용매TetrahydrofuranHCID 8028—
생성물11-Cyclopropyl-5,11-dihydro-4-phenacyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-oneHCID 199600787.2%

반응 단계

To a solution of 11-cyclopropyl-5,11-dihydro-4-methyl-6H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-one (1.0 g) in tetrahydrofuran (25 m L) was added NaH (80% in oil, 0.12 g). The mixture was stirred at room temperature for 30 min. and then cooled to -78° C. Lithium diisopropylamide (1.5 M in cyclohexane, 6.6 mL) was added and the mixture was stirred for an additional 45 min. Benzaldehyde (0.53 g) was added, the mixture was stirred at -65° C. for 1 hour and then allowed to warm to room temperature. The reaction was quenched with water and the volatile materials were removed under reduced pressure. The residue was dissolved in ethyl acetate, washed with water, dried, filtered, and evaporated. The residue was chromatographed over silica gel with 40% ethyl acetate/hexane, and then purified by preparative layer chromatography to give 0.1 g of the title compound, m.p. 195°-197° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620974
출처 데이터셋uspto-grants-1997_04
ORD IDord-8a9ae86ae091467eb912607ba19743bd
출처 메모uspto-grants-1997_04