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- W2952444522 abstract "4-Amino-3-quinolinyl sulfides 4d-e and 7a-c were prepared by amination of 4-chloro-3-quinolinyl sulfides 4c or 1c, respectively, in methanol (140-160 °C) or in boiling phenol with yields up to 95 %. Reaction of 4-dimethylamino-3-quinolinyl sulfides 7c and 4e with nitrating mixture proceeded simultanously as oxidation of the methylthio group to the methylsulfinyl one and as C6-nitration to form 6-nitro-β-quinolinyl sulfoxides 9c or 10b, respectively. 4-Dimethylamino-3-methylsulfinyl-6-nitroquinoline 9c underwent acid catalysed transamination when reacting with primary aliphatic amines and ammonia." @default.
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- W2952444522 date "2008-07-01" @default.
- W2952444522 modified "2023-10-12" @default.
- W2952444522 title "Reactions of 4-dimethylamino-3-quinolinyl sulfides with nitrating mixture and transamination of 4-dimethylamino-3-methylsulfinyl-6-nitroquinoline" @default.
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- W2952444522 doi "https://doi.org/10.1002/jhet.5570450436" @default.
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