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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 12258생성일: 2026년 10월 24일

Naphthalic anhydride → [3-[[3-(1,3-dioxo-3a,9b-dihydro-1H,3H-benzo[de]isoquinolin-2-yl)propyl]methylamino]propyl]carbamic acid tert-butyl ester

https://huagongshe.com/ko/reaction/12258

반응식

참여 물질

역할이름HCID투입량
반응물Naphthalic anhydrideHCID 6693—
반응물tert-butyl N-{3-[(3-aminopropyl)(methyl)amino]propyl}carbamateHCID 12983660—
용매EthanolHCID 702—
생성물[3-[[3-(1,3-dioxo-3a,9b-dihydro-1H,3H-benzo[de]isoquinolin-2-yl)propyl]methylamino]propyl]carbamic acid tert-butyl esterHCID 8661237690%

반응 단계

1,8-naphthalic anhydride (0.18 g, 0.9 mmol) was added to a solution of [3-[(3-aminopropyl)methylamino]propyl]carbamic acid tert-butyl ester previously prepared (Spicer at el., Bioorg. Med. Chem. 2002, vol. 10, p. 19) (0.2 g, 0.8 mmol) in absolute ethanol (20 ml). The reaction mixture was heated at reflux overnight. Removal of the solvent and purification by chromatography on alumina (CH2Cl2/MeOH, 50:1) yielded [3-[[3-(1,3-dioxo-3a,9b-dihydro-1H,3H-benzo[de]isoquinolin-2-yl)propyl]methylamino]propyl]carbamic acid tert-butyl ester (0.37 g, 90%) as a foam.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07728000B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-2a5afcdb095849ddb861073e42e5abbe
출처 메모uspto-grants-2010_06