Potential Anticancer Agents. XIII. Reaction of 3,6-Dimethylpyridazine 1-Oxide and Methylpyridazine 1-Oxides with Benzaldehyde.
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概要
- 論文の詳細を見る
The nucleophilic activity of methyl group in 3,6-dimethylpyridazine 1-oxide (I) and monomethylpyridazine 1-oxides (II) with benzaldehyde was studied. Their corresponding (β-hydroxyphenethyl) pyridazine 1-oxides and styryl compounds were gained. From the results, it may be deduced as follows. (i) The reactivity of 3-and 6-methyl groups in I were almost same, different from the cases of 3,6-dichloropyridazine 1-oxide. (ii) 4- and 6-methyl groups in II were similarly reactive, but 5-methyl was more active, and 3-methyl less active than fore-mentioned two methyl groups. These styryl compounds that were produced respectively, were catalytically hydrogenated with Pd-C to corresponding phenethylpyridazine 1-oxides.
- 公益社団法人日本薬学会の論文
- 1963-09-25
著者
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大草 源三
Showa College of Pharmaceutical Sciences
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板井 孝信
Showa College of Pharmaceutical Sciences
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板井 孝信
National Institute of Hygienic Sciences
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佐子 茂
National Institute of Hygienic Sciences
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大草 源三
National Institute of Hygienic Sciences and Showa Pharmaceutical College
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佐子 茂
National Institute Of Hygienic Sciences:(present Address) Ukima Plant Chugai Pharmaceutical Co. Ltd.
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