Synthesis of Potential Anticancer Agents. VIII. 6-Phenylazo-s-triazolo [2,3-α] pyrimidines.
スポンサーリンク
概要
- 論文の詳細を見る
Several 6-phenylazo-s-triazolo [2,3-α] pyrimidine derivatives were synthesized by either of the following two methods : 1) Benzenediazonium salt was coupled with s-triazolo [2,3-α] pyrimidine derivatives at 6-position, by which the effect of 5- and 7-positions in s-triazolo [2,3-α] pyrimidine was clarified. 2) 2-Phenylazo-1,3-dicarbonyl compounds were condensed with 5-amino-s-triazole (IX).
- 公益社団法人日本薬学会の論文
- 1961-11-25
著者
-
牧角 徳夫
Research Laboratory, Shionogi & Co., Ltd.
-
牧角 徳夫
Shionogi Research Laboratories Shionogi & Co. Ltd.
関連論文
- On the Action of Substituted Azaindolizines on Microorganisms. III. Action of Aminated Azaindolizines on Lactic Acid Bacteria.
- Action of Substituted Azaindolizines on Microorganisms. I. Action on Lactic Acid Bacteria.
- Studies on Fused Indoles. II. Structural Modifications and Analgesic Activity of 4-Aminomethyltetrahydrothiopyrano [2,3-b] indoles
- 2-トリアゾリルシクロアルカノール誘導体の立体および光学異性体の抗菌および植物生長阻害活性
- Synthesis of Potential Anticancer Agents. II. Halogenation of 7-Substituted 5-Methyl-s-triazolo [2,3-a] pyrimidines
- Indole Grignard Reaction. III. : Synthesis, Crystal Structure, and Aalgesic Activity of (R)-and (S)-3-Amino-2,3,4,9-tetrahydrothiopyrano[2,3-b]indoles
- Studies on Fused Indoles. I. Novel Synthesis of 4-Aminomethyltetrahydrothiopyrano [2,3-b] indoles through a Thio-Claisen Rearrangement
- A New Indole Synthesis via Rearrangements of N-Propargylaniline N-Oxides. A One-pot Synthesis of Indole-3-acetonitriles
- The Claisen Rearrangement in Aromatic Heterocyclic Compounds. II. The Thermal Rearrangement of Allyl 4-Quinolyl Ethers
- The Claisen Rearrangement in Aromatic Heterocyclic Compounds. I. The ortho-Claisen Rearrangement of Allyl, Methallyl, and Crotyl Ethers of 2-Methyl-4-quinolinol
- Studies on Azaindolizine Compounds. XVIII. Proton Magnetic Resonance Spectra of s-Triazolo-[1,5-α] pyrimidine and its Derivatives.
- Studies on Azaindolizine Compounds. XVI. The Allyl Rearrangement of 7-Allyloxy-5,6-dimethyls-triazolo [1,5-a] pyrimidime.
- Studies on Azaindolizine Compounds. XV. The Allyl Rearrangement of 5-Methyl-7-allyloxys-triazolo [1,5-a] pyrimidine.
- Studies on Azaindolizine Compounds. XIV. Transetherification in s-Triazolo [1,5-a] pyrimidines.
- Studies on the Azaindolizine Compounds. XIII. Alkylation of 5-Methyl-s-triazolo [1,5-a] pyrimidin-7-ol.
- Studies on the Azaindolizine Compounds. XII. Alkyl Rearrangement of 5-Methyl-7-alkoxy-s-triazolo [1,5-a] pyrimidines.
- Studies on the Azaindolizine Compounds. XI. Synthesis of 6,7-Disubstituted Pyrazolo [1,5-a] pyrimidines.
- Studies on the Azaindolizine Compounds. X. Synthesis of 5,7-Disubstituted Pyrazolo [1,5-a] pyrimidines.
- Synthesis of Potential Anticancer Agents. IX. Condensation of some 2-, 5-, and 7-Methyl-s-triazolo [2,3-α] pyrimidines with Benzaldehyde.
- Synthesis of Potential Anticancer Agents. VIII. 6-Phenylazo-s-triazolo [2,3-α] pyrimidines.
- Synthesis of Potential Anticancer Agents. VII. 6-Nitro- and 6-Amino-s-triazolo [2,3-α] pyrimidines.
- Synthesis of Potential Anticancer Agents. VI. Reactivity of 6-Bromo-s-triazolo [2,3-a] pyrimidines.
- Synthesis of Potential Anticancer Agents. V. 6-Halo-s-triazolo [2,3-a] pyrimidines.
- Synthesis of Potential Anticancer Agents. IV. 5,7-Disubstituted s-Triazolo [2,3-a] pyrimidines.
- Synthesis of Potential Anticancer Agents. III. 7-Substituted s-Triazolo [2,3-a]-pyrimidines and their Halogenated Compounds
- Synthesis of Potential Anticancer Agents. I. 5-Substituted 7-Methyl-s-triazolo [4,3-α]-and-tetrazolo [1,5-α]-pyrimidines.
- Studies on Isoxazole Derivatives. XI. Synthesis of 4-Ethoxycarbonyl-and 4-Cyano-5-aminoisoxazoles and Their Ring Cleavage.
- Isoxazole誘導体の研究(第8報)5-Aminoisoxazole類の接触還元