Studies of Heterocyclic Compounds. VI. The Reactions of 5,6-Dihydrothiazolo [2,3-b] thiazolium Salts with O-and S-Nucleophiles
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概要
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The reaction of 5,6-dihydrothiazolo [2,3-b] thiazolium salts (1) with hydroxide ion furnished disulfide of 3-(2-mercaptoethyl)-4-thiazolin-2-one (6). The reaction of 1 with hydrogensulfide ion furnished 3-(2-mercaptoethyl)-4-thiazolin-2-thione (7) and/or its disulfide (8) and with N, N-dimethyldithiocarbamate ion furnished 3-(N, N-dimethyl-dithiocarbamylethyl)-4-thiazolin-2-thione (12) whereas the reaction of 1b with thiophenolate ion afforded 3-(2-phenylthioethyl)-4-thiazolin-2-thione (18b), thiazole (21), 6b, phenyl 2-[2-(4-phenylthiazolin-2-thion-3-yl) ethylthio] ethyl disulfide (22) and phenyl 2-phenylthioethyl disulfide (23). Brief reaction mechanism of the formation of these products are discussed. The reaction of 1 is considered to be initiated by the attack of the nucleophile on the polarized >C=N< bond to form an adduct and to proceed through AE-mechanism. The elimination stage of the reaction is concluded to depend upon basicity, polarizability and other properties of the reagent to induce either the cleavage of S_7-C_<7a> bond, the cleavage of S_7-C_<7a> and N-C_5 bonds, or another attack of the reagent on C_5 or on S_7.
- 公益社団法人日本薬学会の論文
- 1975-12-25
著者
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宮坂 貞
School of Pharmaceutical Sciences, Showa University
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宮坂 貞
School Of Pharmaceutical Sciences Showa University
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荒川 基一
School of Pharmaceutical Sciences, Showa University
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大塚 宏子
School Of Pharmaceutical Sciences Showa University
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荒川 基一
School Of Pharmaceutical Sciences Showa University
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