Studies on the Syntheses of Hydrogenated Quinolines and Isoquinolines as Analgesics. XII. Synthesis of N-Methyl-7-aza-des-N-morphinan (3-Methyl-5,10b-trimethylene-1,2,3,4,4a, 5,6,10b-octahydrobenzo [f] isoquinoline).
スポンサーリンク
概要
- 論文の詳細を見る
The position of nitrogen in the morphinan skeleton corresponds to the 17-position of D-ring, or 7-position of the C-ring. A synthesis of the morphinan with the nitrogen in this 7-position has been described.
- 社団法人日本薬学会の論文
- 1957-02-20
著者
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杉本 典夫
Osaka Research Laboratory Tanabe Seiyaku Co. Ltd.
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釘田 博至
Osaka Research Laboratory, Tanabe Seiyaku Co., Ltd.
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杉本 典夫
Osaka Research Laboratory Gohei Tanabe & Co. Ltd.
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釘田 博至
Osaka Research Laboratory Tanabe Seiyaku & Co. Ltd.
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釘田 博至
Osaka Research Laboratory Gohei Tanabe & Co. Ltd.
関連論文
- The Preparative and Pharmacological Studies of levo and dextro 9-Aza-des-N-morphinan (2,3,4,4a-Tetrahydro-1H, 6H-5,10b-propanophenanthridin-9-ol).
- Expectorant Effect and Clinical Efficacy of 1-Methyl-3-(di-2-thienylmethylene)piperidine Citrate (AT-327)
- Studies on the Syntheses of Hydrogenated Quinolines and Isoquinolines as Analgesics. XV. Synthesis of 3-Hydroxy-N-methyl-7-aza-des-N-morphinan (9-Hydroxy-3-methyl-5,10b-trimethylene-1,2,3,4,4a, 5,6,10b-octahydrobenzo [f] isoquinoline).
- Studies on the Syntheses of Hydrogenated Quinolines and Isoquinolines as Analgesics. XIV. Synthesis of 6-Hydroxy-4a, 10-trimethylene-1,2,3,4,4a, 9,10,10a-octahydrophenanthridine (Supplement).
- Studies on the Syntheses of Hydrogenated Quinolines and Isoquinolines as Analgesics. XIII. Synthesis of 3-Hydroxy-N-methyl-6-aza-des-N-morphinan (N-Methyl-9-hydroxy-5,10b-trimethylene-1,2,3,4,4a, 5,6,10b-octahydrobenzo [h] isoquinoline).
- Studies on the Syntheses of Hydrogenated Quinolines and Isoquinolines as Analgesics. XII. Synthesis of N-Methyl-7-aza-des-N-morphinan (3-Methyl-5,10b-trimethylene-1,2,3,4,4a, 5,6,10b-octahydrobenzo [f] isoquinoline).
- Studies on the Syntheses of Hydrogenated Quinolines and Isoquinolines as Analgesics. XI. Synthesis of N-Methyl-6-aza-des-N-morphinan (2-Methyl-5,10b-trimethylene-1,2,3,4,4a, 5,6,10b-octahydrobenzo [h] isoquinoline).
- 鎮痛剤としてのHydro化Quinoline類及びIsoquinoline類の合成研究(第9報)3-Hydroxy-N-methyl-16-aza-des-N-morphinanの合成(3-Hydroxy-N-methyl-4b, 9-methanoimino-methano-4b, 5,6,7,8,8a, 9,10-Octahydrophenanthrene)
- 鎮痛剤としてのHydro化Quinoline類及びIsoquinoline類の合成研究(第8報)N-Methyl-16-aza-des-N-morphinanの合成(N-Methyl-4b, 9-methanoiminomethano-4b, 5,6,7,8,8a-9,10-octahydrophenanthrene)
- Syntheses of p-Nitrophenyl Ketones. IV. : Preparation of Some p-Nitrophenyl Alkyl Ketone Derivatives by the Starkey Reaction.
- Structures of Norsecurinine and Dihydronorsecurinine
- Absolute Stereochemistry at C_ of Norsecurinine and Dihydronorsecurinine
- Structure and Stereochemistry of Norsecurinine and Dihydronorsecurinine
- Studies on the Synthetic Analgesics. XVII. Syntheses of 2-(N-tert-Aminoalkylacylamino) thiophene.
- A New Method for Preparation of Alkylnitriles from Alkyl Halide and Alkylammonium Cyanide.
- 合成鎮痛剤の研究-3-
- ピペリヂルカルピノール類の合成研究-1・2-
- Syntheses of Morphine-like Structures. IV. Further Studies on Addition of Borane to 9-Methylenebenzomorphan
- Syntheses of Morphin-like Structures. III. Stereochemical Control of Addition of Borane to 9-Methylenebenzomorphan
- Syntheses of Morphine-like Structures. II. 2'-Methoxy-9-hydroxymethyl-2,5-dimethyl-6,7-benzomorphan
- Syntheses of Morphine-like Structures. I. 9-Hydroxymethyl-2,5-dimethyl-6,7-benzomorphan.
- Studies on Benzoisogranatanine Derivatives. II. Synthesis of 1-Phenethyl-2,4-propano-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinolines.
- Alkylsulfonyltoluene Derivatives (Diuretics. II.).
- Alkylsulfonyltoluene Derivatives (Diuretics. I.).
- 3-Hydroxy-N-methyl-4b, 8a-methanoiminomethano-4b, 5,6,7,8,8a, 9,10-octahydrophenanthreneの合成(鎮痛剤としてのHydro化Quinoline類及びIsoquinoline類の合成研究第7報)
- 鎮痛剤としてのHydro化Quinoline類及びIsoquinoline類の合成研究(第6報)3-Hydroxy-N-methyl-4b, 8a-ethanoiminomethano-4b, 5,6,7,8,8a, 9,10-octahydrophenanthreneの合成
- 鎮痛剤としてのHydro化Quinoline類及びIsoquinoline類の合成研究(第4報)3-Hydroxy-9-azamorphinanの合成
- Benzoisogranatanine Derivatives. I. Synthesis of 2'-Hydroxy-5-alkyl-6,7-benzoisogranatanines.