Benzylcarbonyl化合物とFormamideとの反応(第3報)
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概要
- 論文の詳細を見る
Unlike α-acyl-3,5-dimethoxyphenylacetonitriles, α-acyl-m-methoxyphenylacetonitriles (Ia, b, c, and d) gave 4-amino-5-arylpyrimidines (IIa, b, c, and d) and m-methoxyphenylacetonitrile (III) on being heated with H_2NCHO and POCl_3. In the case of α-benzoyl-m-methoxyphenylacetonitrile (Id), β-amino-α-(m-methoxyphenyl)cinnamonitrile (IV), the intermediate of pyrimidine synthesis, and benzamide (V) were also isolated. III or IV gave IIa or IId under more drastic conditions. Like III, 3,5-dimethoxyphenylacetonitrile (VI) gave 4-amino-5-arylpyrimidine (VII) by analogous treatment.
- 公益社団法人日本薬学会の論文
- 1969-10-25
著者
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廣田 喬
Faculty Of Pharmaceutical Sciences Okayama University
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大和 正利
第一薬科大学
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小山 鷹二
熊本大学薬学部
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戸田 睦子
熊本大学薬学部
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廣田 喬
熊本大学薬学部
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岩井 勝正
熊本大学薬学部
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南 基成
熊本大学薬学部
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