首页> 外国专利> 3-Chloro-5-halo-pyridazine derivs. prepn. - by reacting a 1,3,3,3-tetra:halo-propenyl ketone or aldehyde and cyclising the semicarbazone formed

3-Chloro-5-halo-pyridazine derivs. prepn. - by reacting a 1,3,3,3-tetra:halo-propenyl ketone or aldehyde and cyclising the semicarbazone formed

机译:3-氯-5-卤代哒嗪衍生物。准备-通过使1,3,3,3-四:卤代丙烯基酮或醛反应并环化形成的半脲

摘要

Prepn. of 3-chloro-5-halopyridazines of formula (I):- (where R1 is H, opt. branched 1-5C alkyl or phenyl opt. monosubstd. with Me, Cl, Br or NO2; and R2 is Cl or Br) comprises reacting a cpd. of formula (II):- R1-CO-CR2=CH-CCl3 (II) with semicarbazide or its salt. (I) are intermediates for pharmaceuticals and plant protecting agents. The reaction is simple and (I) is obtd. in high yields. Reaction is at 10-80 (pref. 20-60) degrees C and pH 1-5, pref. in DMF and/or DMSO contg. up to 50 wt. %.
机译:准备式(I)的3-氯-5-卤代哒嗪的通式:-(其中R1为H,优选与Me,Cl,Br或NO2单取代的支链1-5C烷基或苯基; R2为Cl或Br)包括反应一个cpd。式(II)的通式:-R 1 -CO-CR 2 = CH-CCl 3(II)与氨基脲或其盐。 (I)是药物和植物保护剂的中间体。反应很简单,(I)很困难。高产。反应在10-80(优选20-60)摄氏度和pH 1-5(优选)下进行。在DMF和/或DMSO中续。高达50 wt。 %。

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