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N,N-disubstituted derivatives of 3-carboxamide or 3- thiocarboxamide-7-(3- chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1) non ane and preparation II
N,N-disubstituted derivatives of 3-carboxamide or 3- thiocarboxamide-7-(3- chloro-2-propenyl)-1,3,5,7-tetraazabicyclo(3.3.1) non ane and preparation II
Compounds of the formula ##STR1## where X represents O or S and R.sub. 1 and R.sub.2 each represents lower alkyl, phenyl or (lower alkyl)phenyl. The compounds are prepared by reacting the ring-opened intermediate (obtained by reacting cis-1-(3-chloro-2-propenyl)-3,5,7- triaza-1- azoniatricyclo(3.3.1.1.sup.3,7)d ecane chloride with excess aqueous sodium hydroxide) with an equivalent amount of a corresponding carbamoyl halide or thiocarbamoyl halide or at a low temperature to give the indicated tetrasubstituted urea or thiourea product. The compounds have antimicrobial utility.
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机译:分子式为## STR1 ##的化合物,其中X代表O或S,R为代表。 R 1和R 2分别代表低级烷基,苯基或(低级烷基)苯基。通过使开环的中间体(通过使顺式-1-(3-氯-2-丙烯基)-3,5,7-三氮杂-1-氮杂三环(3.3.1.1.sup.3,7)反应而获得的化合物制备乙二胺氯化物和过量的氢氧化钠水溶液)与等量的相应的氨基甲酰卤或硫代氨基甲酰卤或在低温下,得到所示的四取代的脲或硫脲产物。该化合物具有抗菌作用。
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