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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18130생성일: 2026년 10월 25일

5-Isocyanato-1,3-dioxaindane → 1-(1,3-benzodioxol-5-yl)-3-{2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}urea

https://huagongshe.com/reaction/18130

반응식

참여 물질

역할이름HCID투입량
반응물5-Isocyanato-1,3-dioxaindaneHCID 5223213—
반응물11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dioneHCID 10065413—
반응물Dichloromethane methanolHCID 21226129—
용매AcetonitrileHCID 6342—
생성물1-(1,3-benzodioxol-5-yl)-3-{2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}ureaHCID 1671787884%

반응 조건

온도20 °C

반응 단계

A solution of 100 mg (0.30 mmole) of 11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dione (obtained in example 3) in 4 mL of acetonitrile was stirred at 20° C. 3,4-(methylenedioxy)phenyl isocyanate (2 molar equivalents) in 3 mL acetonitrile were added. The mixture was magnetically stirred at 20° C. during 18 hours. The solvent was then evaporated under reduced pressure and the residue was submitted to a flash chromatography on silica (eluent: CH2Cl2/methanol in a 95:5 volume ratio) to provide 125 mg (yield: 84%) of the desired product (formula below) as an orange powder.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741337B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-33b947ef146d494bb67149df97edce5c
출처 메모uspto-grants-2010_06