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Process for the preparation of alkyloxazole derivatives fluorinated on a side chain and novel alkyloxazole derivatives fluorinated on a side chain

机译:侧链氟化的烷基恶唑衍生物和侧链氟化的新型烷基恶唑衍生物的制备方法

摘要

Prepn. of 4-fluoromethyl-5-phenyl-oxazolidine, -oxazoline or oxazolidin-2-one derivs. of formula (I) comprises reacting the corresp. 4-hydroxymethyl cpd. of formula (II) with an alpha , alpha -difluoroalkylamine of formula (III). The novelty is that reaction is carried out at a press. below 2 bars, in presence of an inert solvent which boils above 100 degrees C (under normal press.). X1=H, NO2, alkylthio, etc.; X2=alkyl, haloalkyl, cycloalkyl, etc.; X3=H or as X2; X4=H; or X2+X3=O or X3+X4=bond; Y1=F or Cl; Y2=F, Cl or CF3; Y3,Y4=alkyl; or Y3+Y4=4-5C (un)satd. hydrocarbon chain; alkyl moieties have 1-6C.
机译:准备4-氟甲基-5-苯基-恶唑烷,-恶唑啉或恶唑烷丁-2-酮衍生物。式(I)的化合物包括使对应物反应。 4-羟甲基cpd。式(II)的化合物与式(III)的α,α-二氟烷基胺。新颖之处在于反应是在压力机上进行的。低于2巴,在惰性溶剂中沸点高于100摄氏度(在正常压力下)。 X 1 = H,NO 2,烷硫基等; X 2 =烷基,卤代烷基,环烷基等; X 3 = H或X 2; X 4 = H;或X 2 + X 3 = O或X 3 + X 4 =键;或Y 1 = F或Cl; Y 2 = F,Cl或CF 3; Y 3,Y 4 =烷基;或Y 3 + Y 4 = 4-5C(un)饱和。烃链烷基部分具有1-6C。

著录项

  • 公开/公告号EP0709379A1

    专利类型

  • 公开/公告日1996-05-01

    原文格式PDF

  • 申请/专利权人 BAYER AG;

    申请/专利号EP19950116034

  • 发明设计人 LUI NORBERT DR.;MARHOLD ALBRECHT DR.;

    申请日1995-10-11

  • 分类号C07D263/04;C07D263/10;

  • 国家 EP

  • 入库时间 2022-08-22 03:46:57

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