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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 275278생성일: 2026년 10월 27일

4-Pyridinecarboxylic acid, 1-oxide → 4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)-piperidine N1-oxide

https://huagongshe.com/reaction/275278

반응식

참여 물질

역할이름HCID투입량
반응물4-Pyridinecarboxylic acid, 1-oxideHCID 26130—
반응물Sodium BicarbonateHCID 516892—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물1-Hydroxybenzotriazole hydrateHCID 2796029—
반응물6,11-dihydro-11-(4-piperidinylidene)-5H-imidazo[2,1-b][3]benzazepineHCID 18612492—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)-piperidine N1-oxideHCID 8674848471.3%

반응 조건

온도25 °C

반응 단계

1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (0.61 g) was added to a solution of 6,11-dihydro-11-(4-piperidylidene)-5H-imidazo[2,1-b][3]benzazepine (C, 0.52 g), pyridine-4-carboxylic acid N-oxide (0.44 g) and 1-hydroxybenzotriazole hydrate (0.43 g)in dichloromethane (20 ml) at 0°-5° C. The reaction mixture was then allowed to stir and to warm to 25° C. overnight. Water and 1 M sodium bicarbonate solution were added, and the aqueous layer was extracted with dichloromethane. Combined organic extracts were washed sequentially with water and brine, and were dried, filtered, and concentrated to give 4-(5,6-dihydro-11H-imidazo[2,1-b][3]benzazepin-11-ylidene)-1-(4-pyridinylcarbonyl)-piperidine N1 -oxide (B, 0.54 g), m.p. 155°-159° C. from carbon tetrachloride-dichloromethane. ##STR26##

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05393753
출처 데이터셋uspto-grants-1995_02
ORD IDord-c6dc84e46d104623b15d54e6f9a73627
출처 메모uspto-grants-1995_02