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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18132생성일: 2026년 10월 26일

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-8-yl}urea

https://huagongshe.com/reaction/18132

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참여 물질

역할이름HCID투입량
반응물5-Isocyanato-1,3-dioxaindaneHCID 5223213—
반응물8-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dioneHCID 10065414—
용매AcetonitrileHCID 6342—
생성물1-(1,3-benzodioxol-5-yl)-3-{2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-8-yl}ureaHCID 1671788051%

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온도20 °C

반응 단계

A solution of 100 mg (0.30 mmole) of 8-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dione (obtained in example 4) in 4 mL of acetonitrile was stirred at 20° C. 3,4-(methylenedioxy)phenyl isocyanate (4 molar equivalents) in 3 mL acetonitrile were added. The mixture was magnetically stirred at 20° C. during 24 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 76 mg (yield: 51%). 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-2167b6c38be844559f0a3614f59a5eff
출처 메모uspto-grants-2010_06