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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18139생성일: 2026년 10월 26일

Triethylamine → octyl {2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}carbamate

https://huagongshe.com/reaction/18139

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Carbonochloridic acid, octyl esterHCID 81956—
반응물11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dioneHCID 10065413—
반응물Dichloromethane methanolHCID 21226129—
용매DichloromethaneHCID 6344—
생성물octyl {2-[2-(dimethylamino)ethyl]-1,3-dioxo-2,3-dihydro-1H-dibenzo[de,h]isoquinolin-11-yl}carbamateHCID 1671793693.3%

반응 조건

온도20 °C

반응 단계

100 mg of 11-amino-2-[2-(dimethylamino)ethyl]-1H-dibenzo[de,h]isoquinoline-1,3(2H)-dione (obtained in example 3) (0.30 mmol) were dissolved in 6 ml dichloromethane. 85 μl (2 molar equivalents) of triethylamine and 127 mg (2 molar equivalents) of octyl chloroformate were respectively added. The reaction mixture was maintained at 20° C. for 3 hours. The solvent was then evaporated under reduce pressure and the residue was submitted to a flash chromatography on silica (eluent: CH2Cl2/methanol in a 95/5 volume ratio) to provide 137 mg (yield=85%) 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-eab120ff161a498aafa7ba098af8cad5
출처 메모uspto-grants-2010_06