The Transformation of 3,4-Dihydro-4-quinazolinylmethyl Alkyl Ketones into Quinolines

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概要

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• Both the reactions of 3,4-dihydro-4-quinazolinylmethyl alkyl ketones (4) with active methylene compounds or ketones (NuH) without a catalyst and in the presence of alumina as a catalyst were carried out, and resulted in the transformation of 4 into quinolines (3). Thus 2-(3,4-dihydro-4-quinazolinyl) acetophenone (4a), 2-(3,4-dihydro-4-quinazolinyl)-cyclohexanone (4b), and 1-(3,4-dihydro-4-quinazolinyl)-2-propanone (4c) reacted with diethyl malonate (NuH-2), phenylacetonitrile (NuH-3), acetophenone (NuH-4), cyclopentanone (NuH-5), and cyclohexanone (NuH-6) without catalyst to give 2-phenylquinoline (3b), 1,2,3,4-tetrahydroacridine (3c), and 2-methylquinoline (3d), respectively, together with the dissociation product, quinazoline (1a), although the yield of 3 was very poor. Alumina as a catalyst accelerated these reactions to give 3 in moderate yield. Even the reaction with chloroform (NuH-7) and ethyl orthoformate (NuH-8) gave 3 in good yield. The phenyl and methyl groups substituted at the 2-position prevented 4 from transforming into 3 in both the reactions without a catalyst and in the presence of alumina. A similar transformation was also found between 4,5-dihydro-5-hydroxy-1-methyl-1H-pyrazolo [3,4-d] pyrimidine-4-malononitrile (5) and NuH in the presence of alumina, and resulted in the formation of 6-amino-1-methyl-1H-pyrazolo [3,4-b] pyridine-5-carbonitrile (8). The possible mechanism of the reaction was discussed.

• 公益社団法人日本薬学会の論文
• 1978-11-25

著者

• 林 英作

  Shizuoka College of Pharmacy

• 東野 武郎

  Shizuoka College of Pharmacy

• 林 英作

  School Of Pharmaceutical Sciences University Of Shizuoka

• 鈴木 清

  Shizuoka College of Pharmacy

関連論文

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• Condensed Pyridazines. V. Reactions of 7-(Methylsulfonyl)-1-phenyl-1H-1,2,3-triazolo[4,5-d]pyridazine with Methoxide Ion, Grignard Reagents, Hydrazines, and Amines(Organic,Chemical)
• 縮合環を有するPyridazine誘導体に関する研究(第4報)7-Methoxy-1-phenyl-1H-pyrazolo[3,4-d]pyridazine 5-Oxideの化学的性質
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• 縮合環を有するPyridazine誘導体に関する研究(第2報)5-Phenylpyrido-[2,3-d]pyridazine 7-Oxideの化学的性質
• 縮合環を有するPyridazine誘導体に関する研究(第1報)5,8-Dichloropyrido-[2,3-d]pyridazineとCarbanionとの反応
• Phthalazine誘導体に関する研究(第14報)Phthalazine2-OxideとAcetylenic Dienophileとの反応
• 環状ヒドラジド構造を含む複素環化合物の合成とその抗腫瘍性について
• Grignard Reactions of 1-Phthalazine-, 2-Ouinoxaline-, and 4-Cinnoline-carbonitrile
• Transformation of Quinazoline into 2(1H)-Quinolinones with Alkanoic Anhydrides
• Ring Fission of Quinazolines by Means of the Reissert Reaction
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• Quinoxalines. XXII. Aryl Migration of 2-Aroylquinoxalines to 2-Arylquinoxalines
• Studies on Pyrazolo[3,4-d]pyrimidine Derivatives. XIV. : Preparation and Reactions of 1-Phenyl-1H-pyrazolo-[3,4-d]pyrimidine Reissert Compound
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• Preparation and Reactions of Quinazoline Reissert Compound (3-Benzoyl-3,4-dihydro-4-quinazolinecarbonitrile)
• A Novel Skeletal Rearrangement of Aromatic N-Oxides upon Electron Impact
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• Purines. V. Reaction of 9-Phenyl-9H-purine-6-carbonitrile with Nucleophilic Reagents
• Studies on the Reaction of π-Deficient Heterocycles with Aromatic Aldehyde in the Presence of Cyanide Ion
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• Catalytic Reduction of Heterocyclic Aromatic Amine Oxides with Raney Nickel. II. Reduction of 4-Substituted Quinoline 1-Oxide Derivatives.
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• Catalytic Reduction of Heterocyclic Aromatic Amine N-Oxides with Raney Nickel. IV.^ Reduction of 4,4'-Azopyridine 1,1'-Dioxide, 4,4'-Azoxypyridine 1,1'-Dioxide, and 2-Styrylpyridine 1-Oxide.
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• Triazolo [4,5-d] pyrimidines. IV. The Grignard Reaction of 3-Substituted 3H-1,2,3-Triazolo [4,5-d] pyrimidines
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• Triazolo [4,5-d] pyrimidines. II. On 3-Methyl- and 3-Phenyl-3H-1,2,3-triazolo [4,5-d] pyrimidines
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• Mass Spectra of 3-Alkyl-4-cinnolinecarbonitriles
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• Studies on the Reactions of Pyrido[2,3-d]pyrimidine 3-Oxide with Ketones. The Transformation of Pyrido[2,3-d]pyrimidine 3-Oxide into 1,8-Naphthyridines
• Studies on the Reaction of Quinazoline 3-Oxide with Ketone. The Transformation of Quinazoline 3-Oxide into Quinoline Derivatives
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• On the Reaction of 4-Quinazolinecarbonitrile with Nucleophilic Reagents. III. Reaction of 4-Quinazolinecarbonitrile with Ketones.
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• Studies on 4-Chloropyrido [2,3-d] pyrimidine and Pyrido [2,3-d] pyrimidine
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• Studies on Pyrazolo [3,4-d] pyrimidine Derivatives. IV. On 1-Methyl-and 1-Phenyl-1H-pyrazolo [3,4-d] pyrimidine 5-Oxide

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