1 0 0 0 OA 含窒素環化合物の合成 (第121報)
- 著者
- 高橋 酉蔵 岡田 寿太郎 上田 善子
- 出版者
- 公益社団法人 日本薬学会
- 雑誌
- YAKUGAKU ZASSHI (ISSN:00316903)
- 巻号頁・発行日
- vol.80, no.2, pp.260-264, 1960-02-25 (Released:2010-02-19)
- 参考文献数
- 7
- 被引用文献数
- 1
In order to examine analgesic activity, dimethylaminoethyl and dimethylaminopropyl 6-chloro (methoxy or ethoxy)-2-benzothiazolecarboxylates were prepared. 2-Benzothiazolecarboxylic acids were obtained by the reaction of ethyl 4-chloro (methoxy or ethoxy)-oxanilate and phosphorus pentasulfide to form ethyl thioöxanilates, hydrolyzed with sodium hydroxide to thioöxanilic acids, and cyclized with potassium ferricyanide in alkaline aqueous solution. The acids were derived to the acyl chloride with phosphorus pentachloride and condensed with dimethylaminoethanol or dimethylaminopropanol. These esters underwent decomposition in the air to form 6-chloro-(methoxy or ethoxy)-benzothiazole.Dimethyl- or diethyl-aminoethyl and dimethyl aminopropyl 6-chloro- or 6-ethoxy-2-benzothiazolepropionate were prepared by the application of sulfuric acid in methanol to N-(p-chlorophenyl)- or N-(p-ethoxyphenyl)-succinimide to form methyl succinanilates, reacted with phosphorus pentasuifide to form N-phenylthiosuccinimides, and cyclized with sodium hydroxide to thiosuccinanilic acids, which was further cyclized with potassium ferricyanide to 2-benzothiazolepropionic acids, derived to aryl chlorides with thionyl chloride, and finally condensed with dimethylaminoethanol, dimethylaminopropanol, or diethylaminoethanol.
1 0 0 0 OA 除痛剤の合成 (第13報)
- 著者
- 高橋 酉蔵 堀 幹夫 浜島 好男
- 出版者
- 公益社団法人 日本薬学会
- 雑誌
- YAKUGAKU ZASSHI (ISSN:00316903)
- 巻号頁・発行日
- vol.78, no.1, pp.6-10, 1958-01-25 (Released:2010-02-19)
- 参考文献数
- 18
For the purpose of elucidating the relationship between effective partial structure of morphine skeleton and analgesic action, several compounds possessing the A-C rings in the morphine skeleton as the basic structure were synthesized. The compounds prepared were 1-dimethylaminoalkyl-1-phenylcyclohexanes (XIII, XVIII, XXV, and XXXII) and 2-dimethylaminoalkyl-2-phenylcyclohexanols (XIV, XXI, XXIX, and XXXV).