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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275277생성일: 2026년 10월 26일

Ammonia → 4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)piperidine

https://huagongshe.com/reaction/275277

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물WaterHCID 962—
반응물Phosphorus trichlorideHCID 24387—
반응물4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)-piperidine N1-oxideHCID 86748484—
용매DichloromethaneHCID 6344—
생성물4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)piperidineHCID 15232221—

반응 조건

온도25 °C

반응 단계

A solution of phosphorous trichloride (0.25 ml)in dichloromethane (3 ml) was added to a solution of 4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)-piperidine N1 -oxide (B, 0.4 g) and dichloromethane (5 ml). The reaction mixture was allowed to stir overnight at 25° C. in an atmosphere of nitrogen, and was then poured onto a mixture of ice and water. The resulting mixture was basified with concentrated aqueous ammonia, and the aqueous layer was extracted with dichloromethane. The dried (magnesium sulfate), filtered extracts were concentrated to give 4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene )-1-(4-pyridinylcarbonyl)piperidine (A, 0.34 g), m.p. 207°-209° C. from carbon tetrachloride. ##STR25##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393753
출처 데이터셋uspto-grants-1995_02
ORD IDord-144e1a9cb859414384f4d4df3fd25ea8
출처 메모uspto-grants-1995_02