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Ditercalinium chloride dihydrochloride, NSC-366241(tetramethanesulfonate), RB-1607, NSC-335153

氯化地特卡里Chemical Name: 2,2'-[(4,4'-Bipiperidine)-1,1'-diyldiethylene]bis(10-methoxy-7H-pyrido[4,3-c]carbazolium) dichloride dihydrochloride
CAS No. 74517-42-3 (free base)
项目整合开发状态: Biological Testing
项目研究机构: Bellon (Originator)
合成路线:The reaction of 5-methoxyindole-2-carboxylic acid (I) with thionyl chloride gives the acid chloride (II),which is condensed with dimethylamine to afford the amide (III).Reduction of (III) by LiAlH4 leads to the dimethylamino derivative (IV),which is quaternized by methyl iodide to give (V).The ammonium salt (V) is transformed into the corresponding phosphonium iodide (VI) by means of triphenyl phosphine.The successive steps from (I) to the phosphonium iodide (VI) give an overall yield of 50-60%.The condensation of (VI) with 4-formyl pyridine (VII) gives a mixture of 70% cis-(Z-VIII) and 30% trans-(E-VIII) isomers.The mixture of indolyl-pyridylethylenes (Z-VIII) and (E-VIII) is cyclized to 10-methoxy-7H-pyrido[4,3-c]carbazole (IX) by irradiation for 90 h in a Rayonet photoreactor at 350 nm in the presence of iodine (40% yield).Dimerization of (IX) is achieved by strirring in DMF two equivalents of (IX) with one equivalent of 1,1'-bis(2-chloroethyl)-4,4'-bipiperidine dihydrochloride (X) at 85 C for 18 h and recrystallization in EtOH/H20 (40/60).
📌 参考资料/链接:
参考文献标题:Ditercalinium Chloride
文献作者:Serradell,M.N.; Castar,J.
参考来源:Drugs Fut 1985,10(2),116

📄 详细内容


合成路线:The reaction of 5-methoxyindole-2-carboxylic acid (I) with thionyl chloride gives the acid chloride (II),which is condensed with dimethylamine to afford the amide (III).Reduction of (III) by LiAlH4 leads to the dimethylamino derivative (IV),which is quaternized by methyl iodide to give (V).The ammonium salt (V) is transformed into the corresponding phosphonium iodide (VI) by means of triphenyl phosphine.The successive steps from (I) to the phosphonium iodide (VI) give an overall yield of 50-60%.The condensation of (VI) with 4-formyl pyridine (VII) gives a mixture of 70% cis-(Z-VIII) and 30% trans-(E-VIII) isomers.The mixture of indolyl-pyridylethylenes (Z-VIII) and (E-VIII) is cyclized to 10-methoxy-7H-pyrido[4,3-c]carbazole (IX) by irradiation for 90 h in a Rayonet photoreactor at 350 nm in the presence of iodine (40% yield).Dimerization of (IX) is achieved by strirring in DMF two equivalents of (IX) with one equivalent of 1,1'-bis(2-chloroethyl)-4,4'-bipiperidine dihydrochloride (X) at 85 C for 18 h and recrystallization in EtOH/H20 (40/60).

参考文献标题:DNA intercalating comnpounds as potential antitumor agents.1.Preparation and properties of 7H-pyridocarbazoles
文献作者:Pelaprat,D.; Oberlin,R.; Le Guen,I.; Roques,B.P.; Le Pecq,J.B.
参考来源:J Med Chem 1980,23(12),1330-1335


合成路线:The reaction of 5-methoxyindole-2-carboxylic acid (I) with thionyl chloride gives the acid chloride (II),which is condensed with dimethylamine to afford the amide (III).Reduction of (III) by LiAlH4 leads to the dimethylamino derivative (IV),which is quaternized by methyl iodide to give (V).The ammonium salt (V) is transformed into the corresponding phosphonium iodide (VI) by means of triphenyl phosphine.The successive steps from (I) to the phosphonium iodide (VI) give an overall yield of 50-60%.The condensation of (VI) with 4-formyl pyridine (VII) gives a mixture of 70% cis-(Z-VIII) and 30% trans-(E-VIII) isomers.The mixture of indolyl-pyridylethylenes (Z-VIII) and (E-VIII) is cyclized to 10-methoxy-7H-pyrido[4,3-c]carbazole (IX) by irradiation for 90 h in a Rayonet photoreactor at 350 nm in the presence of iodine (40% yield).Dimerization of (IX) is achieved by strirring in DMF two equivalents of (IX) with one equivalent of 1,1'-bis(2-chloroethyl)-4,4'-bipiperidine dihydrochloride (X) at 85 C for 18 h and recrystallization in EtOH/H20 (40/60).

参考文献标题:DNA intercalating comnpounds as potential antitumor agents.2.Preparation and properties of 7H-pyridocarbazole dimers
文献作者:Pelaprat,D.; Delbarre,A.; Le Guen,I.; Roques,B.P.; Le Pecq,J.B.
参考来源:J Med Chem 1980,23(12),1336-1343


合成路线:The reaction of 5-methoxyindole-2-carboxylic acid (I) with thionyl chloride gives the acid chloride (II),which is condensed with dimethylamine to afford the amide (III).Reduction of (III) by LiAlH4 leads to the dimethylamino derivative (IV),which is quaternized by methyl iodide to give (V).The ammonium salt (V) is transformed into the corresponding phosphonium iodide (VI) by means of triphenyl phosphine.The successive steps from (I) to the phosphonium iodide (VI) give an overall yield of 50-60%.The condensation of (VI) with 4-formyl pyridine (VII) gives a mixture of 70% cis-(Z-VIII) and 30% trans-(E-VIII) isomers.The mixture of indolyl-pyridylethylenes (Z-VIII) and (E-VIII) is cyclized to 10-methoxy-7H-pyrido[4,3-c]carbazole (IX) by irradiation for 90 h in a Rayonet photoreactor at 350 nm in the presence of iodine (40% yield).Dimerization of (IX) is achieved by strirring in DMF two equivalents of (IX) with one equivalent of 1,1'-bis(2-chloroethyl)-4,4'-bipiperidine dihydrochloride (X) at 85 C for 18 h and recrystallization in EtOH/H20 (40/60).
参考文献标题:
文献作者:Bible,R.; Yuan,J.J.; Yang,D.-C.; Zhang,J.Y.; Findlay,J.W.; Karim,A.
参考来源:Compt Rend Acad Sci 1976,283(9),1109-1112


产品链接: CAS No. 74517-42-3››