908084-32-2

Basic information

• Product Name: 6-benzyl-2,3-dimethoxy-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione
• Synonyms: 6-benzyl-2,3-dimethoxy-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione
• CAS NO: 908084-32-2
• Molecular Weight: 397.43
• Mol File: 908084-32-2.mol

Chemical Properties

• CAS DataBase Reference: 6-benzyl-2,3-dimethoxy-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 6-benzyl-2,3-dimethoxy-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione(908084-32-2)
• EPA Substance Registry System: 6-benzyl-2,3-dimethoxy-5H-indeno[1,2-c]isoquinoline-5,11(6H)-dione(908084-32-2)

Safety Data

• Hazardous Substances Data: 908084-32-2(Hazardous Substances Data)

Upstream product

• 606-23-5 1H-indene-1,3(2H)-dione 
• 490-64-2 asaronic acid 
• 791796-85-5 C₁₇H₁₉NO₄ 
• 1384384-90-0 C₂₅H₂₁NO₄ 
• 1384384-88-6 C₂₅H₂₁NO₄ 
• 1384384-83-1 C₂₅H₂₃NO₄ 
• 1384384-85-3 C₁₉H₂₁NO₅ 

Relevant articles and documents

Synthesis of Biologically Active Indenoisoquinoline Derivatives via a One-Pot Copper(II)-Catalyzed Tandem Reaction

A concise route for the synthesis of indenoisoquinoline derivatives from 2-iodobenzamide and 1,3-indanedione derivatives in the presence of copper(II) chloride and cesium carbonate in acetonitrile solvent is reported. A wide variety of 2-iodobenzamide derivatives and indandiones could be used to synthesize indenoisoquinoline derivatives and other fused indenoisoquinoline in moderate to good yields. This methodology was adapted for the one-step synthesis of a series of clinically active topoisomerase I inhibitors such as NSC 314622, LMP-400, LMP-776.

Preparation method of indenoisoquinoline derivative

The invention relates to a preparation method of an indenoisoquinoline derivative as shown in formula (I). The preparation method includes the steps of (A), providing a first reactant as shown in formula (II) and a second reactant as shown in formula (III

METHOD FOR PREPARING INDENOISOQUINOLINE DERIVATIVES

A method for preparing indenoisoquinoline derivatives represented by the following formula (I) is disclosed, which comprises the following steps: (A) providing a first reactant represented by the following formula (II) and a second reactant represented by the following formula (III): wherein, R1, R3, A, X, Y, Z, m and n are defined in the specification; and (B) reacting the first reactant represented by the formula (II) and the second reactant represented by the formula (III) in a solvent and selectively adding R2NH2 therein, to obtain the indenoisoquinoline derivatives represented by the formula (I).

Photochemically induced synthesis of the topoisomerase i inhibitors indeno [1,2-c]isoquinoline-5,11-diones

A convenient synthesis of indeno[1,2-c]isoquinoline-5,11-diones has been achieved using combinational photochemical and carbocationic cyclization tactics. The synthetic route involved first the construction of adequately functionalized N-styryl benzamides via Suzuki-Miyaura cross-coupling reaction with enol phosphate combined with a six - electron photocyclization process. The assembling of the title compounds was readily ensured through sequential carbocationic annulation reaction and ultimate oxidation of a latent hydroxy functionality. Georg Thieme Verlag Stuttgart · New York.