Studies on the Syntheses of N-Heterocyclic Compounds. V. 2-Aryl-5,8-dichloropyrimido [4,5-d] pyridazine
スポンサーリンク
概要
- 論文の詳細を見る
2-Substituted-5,6,7,8-tetrahydropyrimido [4,5-d] pyridazine-5,8-diones (6) having a variety of substituents at 2-position were synthesized. Chlorination reaction of 6 were carried out, and it was found that only the compound which have aryl substituent at 2-position could be converted to 2-aryl-5,8-dichloropyrimido [4,5-d] pyridazine (14), while other derivatives gave no corresponding dichlorides (14). 2,4-Diphenyl-5,6,7,8-tetra-hydropyrimido [4,5-d] pyridazine-5,8-dione (9) was not obtained because of its structural unstability caused by steric interference of phenyl group at 4-position.
- 公益社団法人日本薬学会の論文
- 1972-07-25
著者
-
万木 庄次郎
武田薬品中研
-
川松 豊
干寿製薬株式会社経営戦略室
-
冨本 光美
京大(医)衛生学
-
杉原 弘貞
Chemistry Research Laboratories, Takeda Chemical Industries, Ltd.,
-
杉原 弘貞
Central Research Division Takeda Chemical Industries. Ltd.
-
川松 豊
Chemical Research Laboratories, Central Research Division, Takeda Chemical Industries, Ltd.
-
万木 庄次郎
Chemical Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd.
-
稗田 勝
Chemical Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd.
-
伏見 富吉
Chemical Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd.
-
冨本 光美
Chemical Research Laboratories, Research and Development Division, Takeda Chemical Industries, Ltd.
-
稗田 勝
武田薬品工業株式会社, 研究開発本部, 化学研究所
-
稗田 勝
武田薬品工業株式会社 研究開発本部 化学研究所
-
伏見 富吉
武田薬品工業株式会社 中央研究所 化学研究所
関連論文
- Synthesis and Angiotensin Converting Enzyme-Inhibitory Activity of 1,5-Benzothiazepine and 1,5-Benzoxazepine Derivatives. III
- Synthesis and Angiotensin converting Enzyme Inhibitory Activity of 1,5-Benzothiazepine and 1,5-Benzoxazepine Derivatives. II
- Synthesis and Angiotensin Converting Enzyme Inhibitory Activity of 1,5-Benzothiazepine and 1,5-Benzoxazepine Derivatives. I
- Structure-Activity Relationships of the Diuretic Activity of Triaza- and Tetraaza-naphthalene Compounds
- 2.チオクロムリン酸エステルに関する研究(第1報)(ビタミンB研究委員会 : 第245回会議研究発表要旨)
- 1,5-Benzoxathiepin Derivatives. II. Synthesis and Serotonin S_2-Receptor-BIocking Activity of Aminoalkyl-Substituted 3,4-Dihydro-2H-1,5-benzoxathiepin-3-ols and Related Compounds(Medicinal Chemistry,Chemical)
- 1,5-Benzoxathiepin Derivatives. I. Synthesis and Reaction of 1,5-Benzoxathiepin Derivatives(Medicinal Chemistry,Chemical)
- インスリン抵抗性改善薬ピオグリタゾンの創製
- Studies on Antidiabetic Agents. VII. : Synthesis and Hypoglycemic Activity of 4-Oxazoleacetic Acid Derivatives
- Studies on Antidiabetic Agents. II. Synthesis of 5-[4-(1-Methylcyclohexylmethoxy)-benzyl] thiazolidine-2,4-dione (ADD-3878) and Its Derivatives
- Studies on Antidiabetic Agents. I. Synthesis of 5-[4-(2-Methyl-2-phenylpropoxy)-benzyl] thiazolidine-2,4-dione (AL-321) and Related Compounds
- Syntheses and β-Adrenoceptor Activities of 2-Alkylamino-6-hydroxy-5-hydroxymethyl-1,2,3,4-tetrahydro-1-naphthalenols
- The Syntheses and β-Adrenoceptor Activities of N-Substituted 2-Amino-5,6-dihydroxy-1,2,3,4-tetrahydro-1-naphthalenols
- New 1,4-Dihydropyridine Derivatives with Potent and Long-Lasting Hypotensive Effect
- Studies on Antidiabetic Agents. VI. Asymmetric Transformation of (±)-5-[4-(1-Methylcyclohexylmethoxy) benzyl]-2,4-thiazolidinedione (Ciglitazone) with Optically Active 1-Phenylethylamines
- Studies on Antidiabetic Agents. IV. Synthesis and Activity of the Metabolites of 5-[4-(1-Methylcyclohexylmethoxy) benzyl]-2,4-thiazolidinedione (Ciglitazone)
- Antiulcer Activity of 5-Benzylthiazolidine-2,4-dione Derivatives
- Studies on Antidiabetic Agents. III. 5-Arylthiazolidine-2,4-diones as Potent Aldose Reductase Inhibitors
- 1,5-Benzoxathiepin Derivatives. III. Optical Resolution of Methyl (±)-cis-3-Hydroxy-4-[3-(4-phenyl-1-piperazinyl)propyl]-3,4-dihydro-2H-1,5-benzoxathiepin-4-carboxylate Hydrochloride ((±)-CV-5197) with Selective 5-Hydroxytryptamine_2(5-HT_2)-Antagonistic
- Syntheses of 6-Amino-1,2-dihydroxy-6,7,8,9-tetrahydro-5H-benzocyclohepten-5-ol Derivatives
- Studies on the Syntheses of N-Heterocyclic Compounds. XXVIII. Syntheses of Pyrido [3,4-d] pyridazine Derivatives. (4)
- Studies on the Syntheses of N-Heterocyclic Compounds. XXVI. Syntheses of Pyrido [3,4-d] pyridazine Derivatives. (3)
- Studies on the Syntheses of N-Heterocyclic Compounds. XXV. Syntheses of Pyrido [3,4-d] pyridazine Derivatives. (2)
- Studies on the Syntheses of N-Heterocyclic Compounds. XXIV. Oxidation of Dihydrotetraazanaphthalene Derivatives
- Studies on the Syntheses of N-Heterocyclic Compounds. XXII. The Reaction of Polyazanaphthalene Derivatives with Organometallic Reagents
- Syntheses of 1,2-N-Alkylimino-1,2,3,4-tetrahydronaphthalene Derivatives and Preparation of Ring Closed Analog of Salbutamol as a New β-Adrenoceptor Agent
- Spirocyclopropane Compounds. III. Synthesis of Spiro [benzofuran-2 (3H), 1'-cyclopropan]-3-ones for Evaluation as Gastric Antisecretory and Antiulcer Agents
- Studies on the Syntheses of N-Heterocyclic Compounds. IV. Hypocholesterolemic 1,2,4-Oxadiazole Derivatives. (2)
- Studies on the Synthese of N-Heterocyclic Compounds. III. Hypocholesterolemic 1,2,4-Oxadiazole Derivatives (1)
- チオクロムリン酸エステル類の合成と螢光特性
- Chemistry of Salicylic Acid and Anthranilic Acid. I. Reduction of Methyl Salicylate, Methyl Anthranilate and Their Derivatives with Sodium Borohydride
- Chemistry of Salicylic Acid and Anthranilic Acid. II. Formation of 2-Alkyl-3-(2-carboxyphenyl)-4-quinazolone from 2-Alkyl-4-oxo-4H-3,1-benzoxazine by Dimeric Condensation
- Decomposition of Thiamine in Alcohol Solution. II
- Pyrrolo[1,2-α]indole誘導体の合成
- Studies on the Syntheses of N-Heterocyclic Compounds. VII. 2-Aryl-5,8-disubstitutedpyrimido [4,5-d] pyridazine
- Studies on the Syntheses of N-Heterocyclic Compounds. V. 2-Aryl-5,8-dichloropyrimido [4,5-d] pyridazine
- 含窒素複素環式化合物の合成研究(第12報)Pyrido[3,4-d]pyridazineおよびPyrido[2,3-d]pyridazine誘導体の合成
- 含窒素複素環式化合物の合成研究(第10報)2-Phenyl-pyrazino-[2,3-d]pyridazine誘導体の合成
- 含窒素複素環式化合物の合成研究(第9報)2-Aryl-5,8-disubstituted Pyrimido[4,5-d]pyridazineの還元について
- 含窒素複素環式化合物の合成研究(第8報)2-Phenylpyrimido-[4,5-d]Pyridazine誘導体の加水分解
- Studies on the Syntheses of N-Heterocyclic Compounds. VI. Monosubstitution of 2-Phenyl-5,8-dichloropyrimido [4,5-d] pyridazine
- チオクロム及びそのリン酸エステルの蛍光特性について : 日本ビタミン学会第31回大会研究発表要旨
- Syntheses of conformationally Rigid Catecholamine Derivatives
- Studies on the Syntheses of N-Heterocyclic Compounds. XXIII. The Photochemical Reaction of Polyazanaphthalene Derivatives
- 含窒素複素環式化合物の合成研究(第19報)4-Alkyl-5,8-disubstituted Amino-2-phenyl-3,4-dihydropyrimido[4,5-d]pyridazineの合成
- 含窒素複素環式化合物の合成研究(第14報)7-Phenyl-s-triazolo-[4,3-α]pyridine誘導体の合成
- 含窒素複素環式化合物の合成研究(第11報)3-Phenyl-pyridazino[4,5-c]-および5-Phenyl-pyridazino[4,5-d]pyridazine誘導体の合成
- Studies on the Syntheses of N-Heterocyclic Compounds. II. Pyrimido[4,5-e]-, Pyridazino[3,4-e]- and Pyrido[4,3-e]-1,2,3,5-tetrahydro[1,4]oxazepine-5-one
- Hydroxyethylthiamine同族体およびこれらのDiacyl誘導体の合成 : ビタミンB_1および諸関係化合物の研究(CV)
- Spirocyclopropane Compounds. VI. : Synthesis of Spiro[benzo[b]-thiophene-2(3H), 1'-cyclopropan]-3-ones
- Stereoselective Syntheses of cis- and trans-2-Alkylamino-1,2,3,4-tetrahydro-1-naphthalenols by Acid-catalyzed Ring Opening of 1,2-N-Alkylimino-1,2,3,4-tetrahydronaphthalenes
- 14 イソプレノイドキノン類の合成
- Sterische Struktur der Giftstoffe aus dem Fruchtfleisch von Ginkgo biloba L.
- An Improved Synthesis of the New Angiotensin Converting Enzyme Inhibitor CV-5975 via a Chemoenzymatic Process(Organic,Chemical)
- 12.チアゾール核2位置換ビタミンB_1誘導体(I) : Hydroxyethylthiamine関連化合物(第155回会議研究発表要旨)
- 103.Carnitine誘導体の合成(第13回大会研究発表要旨)
- S-Acylthiamine誘導体の合成と安定性