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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2196084생성일: 2026년 10월 26일

Methanol → 1-Ethyl-3,3,5-trimethyl-7-{3-[(pyridin-4-ylmethyl)amino]propoxy}-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione

https://huagongshe.com/reaction/2196084

반응식

참여 물질

역할이름HCID투입량
반응물MethanolHCID 887—
반응물4-PyridinecarboxaldehydeHCID 13389—
반응물Sodium borohydrideHCID 4311764—
반응물7-(3-Aminopropoxy)-1-ethyl-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dioneHCID 68673521—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물1-Ethyl-3,3,5-trimethyl-7-{3-[(pyridin-4-ylmethyl)amino]propoxy}-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dioneHCID 6867280284.2%

반응 단계

4-Pyridinecarbaldehyde (0.64 ml, 6.8 mmol) was added to a methanol solution (10 ml) of 7-(3-aminopropoxy)-1-ethyl-3,3,5-trimethyl-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione (2.18 g, 6.8 mmol), and stirred under a nitrogen atmosphere at room temperature for 1.5 hours. The reaction mixture was cooled in an ice water bath, and sodium borohydride (257 mg, 6.8 mmol) was added thereto at 0° C. The mixture was then stirred at room temperature overnight. Water was added to the reaction mixture, and extraction with ethyl acetate was performed. The organic layer was washed with water and a saturated sodium chloride aqueous solution, in this order, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate:methanol=9:1→3:2). The purified product was concentrated under reduced pressure to thereby obtain 2.35 g (yield: 84%) of 1-ethyl-3,3,5-trimethyl-7-{3-[(pyridin-4-ylmethyl)amino]propoxy}-1,5-dihydrobenzo[b][1,4]diazepine-2,4-dione as a pale yellow oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08338406B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-f117cbcccedf42c3a149dff2ea696f80
출처 메모uspto-grants-2012_12