Studies on Syntheses and Reactions of Methoxypyridazines. I. Methoxylation of 3,4,5-Trichloropyridazine(Organic,Chemical)
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The reaction of 3,4,5-trichloropyridarine (1) with 1 eq amount of NaQMe resulted in the formation of three dichloromonomethoxypyridazines (2,3-OMe; 3,4-OMe; 4,5-OMe) in the ratio of 1:3:6. The 4-OMe compound 3 was isolated from the reaction mixture and the 3-OMe compound 2 was synthesized independently. Further methoxylation of 2, 3 and 4 was also investigated in order to prepare various substituted pyridazines.
収録刊行物
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- Chemical & pharmaceutical bulletin
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Chemical & pharmaceutical bulletin 35 (1), 421-424, 1987-01-25
公益社団法人日本薬学会
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詳細情報 詳細情報について
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- CRID
- 1571698602255256192
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- NII論文ID
- 110006280917
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- NII書誌ID
- AA00602100
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- ISSN
- 00092363
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- 本文言語コード
- en
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- データソース種別
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- CiNii Articles