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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 54758생성일: 2026년 10월 24일

Sodium Iodide → 5-(2-cyanomethylaminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine

https://huagongshe.com/ko/reaction/54758

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물ChloroacetonitrileHCID 7856—
반응물TriethylamineHCID 8471—
반응물5-(2-aminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepineHCID 18917210—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물5-(2-cyanomethylaminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepineHCID 53719122—

반응 조건

온도60 °C

반응 단계

0.01 ml of chloroacetonitrile, 0.22 ml of triethylamine and 0.24 ml of sodium iodide were added to 50 ml of a solution of 0.7 g of 5-(2-aminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzoazepine dissolved in dimethylformamide. The mixture was stirred at 60° C. for 2 hours. The reaction mixture was mixed with water, followed by extraction with ethyl acetate-n-hexane (10:1). The organic layer was water-washed, dried and subjected to vacuum distilation to remove the solvent. The residue was purified by silica gel column chromatography (elutant: dichloromethane/methanol=50/1) and crystallized from acetone-n-hexane to obtain 0.5 g of 5-(2-cyanomethylaminoethoxy)-7-chloro-1-[2-methoxy-4-(2-chlorobenzoylamino)benzoyl]-2,3,4,5-tetrahydro-1H-benzo-azepine.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05622947
출처 데이터셋uspto-grants-1997_04
ORD IDord-1e51edf5b77046b28bfbebbd9e96e5e4
출처 메모uspto-grants-1997_04