113809-07-7

Upstream product

• 481-39-0 5-hydroxynaphtho-1,4-quinone 
• 65899-49-2 1(E)-<(benzyloxycarbonyl)amino>-1,3-butadiene 

Downstream Products

• 113809-10-2 (5-Hydroxy-9,10-dioxo-9,10-dihydro-anthracen-1-yl)-carbamic acid benzyl ester 
• 113809-12-4 (8-Hydroxy-9,10-dioxo-9,10-dihydro-anthracen-1-yl)-carbamic acid benzyl ester 
• 113809-11-3 (5-Methoxy-9,10-dioxo-9,10-dihydro-anthracen-1-yl)-carbamic acid benzyl ester 
• 113809-13-5 Acetic acid 8-benzyloxycarbonylamino-9,10-dioxo-9,10-dihydro-anthracen-1-yl ester 

Relevant academic research and scientific papers

AN EFFICIENT ROUTE TO AMINOANTHRAQUINONES AND DERIVATIVES VIA A DIELS-ALDER REACTION.

Cycloadditions of (E)-1-N-carbobenzoxyamino-1,3-butadiene to naphtoquinones followed by aromatization of the adducts and deprotection of the amino group afford regioselective syntheses of -5 and -8 substituted aminoanthraquinones.

Diels-Alder reactions between dienamides and quinones: Stereochemistry of the cycloadditions and cytotoxic activity of the adducts

Tetrahydronaphthoquinones and tetrahydroanthraquinones bearing an amido group have been prepared by Diels-Alder reactions between (E)-1-(N-carbobenzyloxyamino)-1,3-butadiene (2) or (E)-1-(N-benzoyl-N-benzylamino)-1,3-butadiene (5) and benzoquinone or 5-substituted naphthoquinones. The stereochemistry of the cycloadditions was investigated. A high regioselectivity was observed in the reaction of the diene carbamate 2 with 5-methoxy and 5-acetoxy naphthoquinones. This latter gave the unexpected 1,8-regioisomer 3d. The cycloadditions of the dienamide 5 with naphthoquinones 1 (R = OH, OMe, OAc) are regiospecific. Assignment of the structure of the tetrahydroanthraquinone 6b is in good agreement with the known directing effect of the 5-hydroxy group of juglone 1b in analogous Diels-Alder reactions. With 5-methoxy and 5-acetoxy naphthoquinones, the opposite regiochemistry observed is consistent with the electron-donating influence of the methoxy or acetoxy group, making the C-3 carbon atom more electron deficient. Aromatization of the adducts 6b and 7c was accompanied by an unusual elimination of the amido moiety. Thus, 1-hydroxy and 1-methoxy anthraquinones were obtained. Reactions of the dienes 2 and 5 with benzoquinone gave the tetrahydronaphthoquinones 9 and 10 with an endo stereospecificity. Oxidation of 9 by activated manganese dioxide gave the naphthoquinone 11. These compounds were submitted to in vitro cytotoxic assays towards murine L 1210 leukemia cells and clonogenic human tumor cell line MDA-MB 231. The naphthoquinone derivatives 9, 10 and 11 had significant activities with IC50 ≤ 0.4 μg/ml towards these two tumor cell systems.