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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 540312생성일: 2026년 10월 24일

Phosphorus oxychloride → 2-Chloro-6-{[1-(1,3,4,5-tetrahydro-2H-2-benzazepin-2-yl)ethylidene]amino}benzonitrile

https://huagongshe.com/ko/reaction/540312

반응식

참여 물질

역할이름HCID투입량
반응물Phosphorus oxychlorideHCID 24813—
반응물2-Amino-6-chlorobenzonitrileHCID 81056—
반응물Sodium BicarbonateHCID 516892—
반응물1-(1,3,4,5-Tetrahydro-2H-2-benzazepin-2-yl)ethanoneHCID 10465110—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
생성물2-Chloro-6-{[1-(1,3,4,5-tetrahydro-2H-2-benzazepin-2-yl)ethylidene]amino}benzonitrileHCID 7125458963.9%

반응 단계

Phosphorus oxychloride (2.93 mL, 32.0 mmol) was added to a stirred solution of 1-(1,3,4,5-tetrahydro-2H-2-benzazepin-2-yl)ethanone (5.5 g, 29.0 mmol) in dry dichloromethane (100 mL) at 10° C. After that, the mixture was stirred for 20 minutes at room temperature. Then a solution of 2-amino-6-chloro-benzonitrile (4.43 g, 29.0 mmol) in dry dichloromethane (40 mL) was added and the resulting suspension was heated under reflux for 24 hours. After the reaction mixture was cooled to room temperature, water (50 mL) was added followed by saturated sodium bicarbonate to pH 8. The organic layer was separated and the aqueous was extracted with dichloromethane (100 mL). The organic fraction was washed with brine and dried over sodium sulfate, and then evaporated in vacuo to give a residue which was precipitated in ether. The solid was collected by filtration and dried in vacuo to give 6 g of product as a brown powder (yield was 63.7%). It was used in the next step without further purification. MS obsd. (ESI+) [(M+H)+] 324.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08871756B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-1a12b80a46b04bebbaefe099bf976c4b
출처 메모uspto-grants-2014_10