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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 9717생성일: 2026년 10월 24일

Acetonitrile → 10-methoxy-5H-dibenz(b,f)azepine-5-carboxamide

https://huagongshe.com/ko/reaction/9717

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물10-MethoxyiminostilbeneHCID 78424—
반응물Benzenesulfonic acid, 4-methyl-, compd. with pyridine (1:1)HCID 466102—
반응물HCID 178418852HCID 178418852—
용매WaterHCID 962—
생성물10-methoxy-5H-dibenz(b,f)azepine-5-carboxamideHCID 12003150.7%

반응 단계

10-methoxy-5H-dibenz(b,f)azepine (29.9 g, 0.134 mol) was added to 300 ml acetonitrile in a three-neck flask (500 ml) equipped with a mechanical stirring apparatus. The mixture was stirred at room temperature for 15 minutes, and then NaOCN (18 g, 0.277 mol) was added, followed by pyridinium p-toluenesulfonate (75 g, 0.3 mol). The mixture was stirred at room temperature for about 4 hours, at which time TLC indicated that the reaction was complete (disappearance of 10-methoxy-5H-dibenz(b,f)azepine). 30 ml water was added, and the mixture stirred for 15 minutes. The solids were filtered and the filtrate was concentrated under vacuum. The semi-solid residue was triturated with acetone to provide a creamy solid, which was dried at 80° C. to provide 18 g (0.068 mol, 50% yield) of 10-methoxy-5H-dibenz[b,f]azepine-5-carboxamide (10-methoxycarbamazepine).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091339B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-ce0dd8900c0f4904b3ae6c61be0151bc
출처 메모uspto-grants-2006_08