📜3,4-吡啶二羧酸置于乙酸酐体系中,用 二氯甲烷 用作溶剂,化学反应 19.0H,反应生成3-羧酸-4-羧酸甲酯吡啶
参考文献:Synthesis Of 11-Amino-Substituted-9-Methoxy-5-Methyl-6H-Pyrido[4,3-B]-Carbazoles
标题:Synthesis Of 11-Amino-Substituted-9-Methoxy-5-Methyl-6H-Pyrido[4,3-B]-Carbazoles
摘要:A Route To 11-Amino-Substituted-6H-Pyrido[4,3-B]Carbazoles Has Been Studied. Thus,Condensation Of 2-(4-Lithiopyridine-3-yl)-4,4-Dimethyloxazoline With 2-Acetyl-5-Methoxy-1-Phenylsulphonylindole Led To A Low Yield Of The Expected Alcohol,Which Upon Hydrolysis Gave A Complex Mixture. A Better Starting Building Block Was 4-Acetyl-N,N-Diisopropylnicotinamide Obtained Either From N,N-Diisopropyl-4-Lithionicotinamide (Low Yield) Or From Pyridine-3,4-Dicarboxylic Anhydride,Using A 4-Step Sequence. This Compound Was Treated With 2-Lithio-5-Methoxy-1-Phenylsulphonylindole,Affording N,N-Diisopropyl-4-[1-(5-Methoxy-1-Phenylsulphonylindol-2-yl)-1-Hydroxyethyl]Nicotinamide. Hydrolysis And Then Reduction Led To 4-[1-(5-Methoxy-1-Phenylsulphonylindol-2-yl)-Ethyl]Nicotinic Acid Whose Amides Were Cyclized By Phosphorus Trichlorideoxide. Finally,The Title Compounds Were Obtained By Raney-Nickel Reduction-Elimination Of The 6-Phenylsulphonyl Protecting Group.
Doi:10.1039/p19910003165