where R - hydrogen, lower alkyl or a group of the formula (II) or (III) where R1-CHO or -CN. Reagent 1: compound of the formula (IV) where R as indicated above; R3 - benzyl. Reagent 2: halogenating agent, preferably sulfuryl chloride. Reagents 1 and 2 after interaction form compound of the formula (V) which is subjected for interaction with ammonia, preferably at the room temperature. Compound of the formula (IV) is synthesized from the compound of the formula (VI) and benzylmercaptan in the medium of aprotonic organic solvent. Synthesized products were used as intermediate compounds for synthesis of pharmaceutically active substances. EFFECT: improved method of synthesis. 6 cl"/> METHOD OF SYNTHESIS OF 6-FLUORO-1,2-BENZISOTHIAZOLE, ORTHO-SUBSTITUTED PHENACYL-DERIVATIVE, AND A METHOD OF ITS SYNTHESIS
首页> 外国专利> METHOD OF SYNTHESIS OF 6-FLUORO-1,2-BENZISOTHIAZOLE, ORTHO-SUBSTITUTED PHENACYL-DERIVATIVE, AND A METHOD OF ITS SYNTHESIS

METHOD OF SYNTHESIS OF 6-FLUORO-1,2-BENZISOTHIAZOLE, ORTHO-SUBSTITUTED PHENACYL-DERIVATIVE, AND A METHOD OF ITS SYNTHESIS

机译:6-氟-1,2-苯并异噻唑,邻位取代的苯甲酰基衍生物的合成方法及其合成方法

摘要

FIELD: organic chemistry. SUBSTANCE: product - 6-fluoro-1,2- benzoisothiazoles of the formula (I) where R - hydrogen, lower alkyl or a group of the formula (II) or (III) where R1-CHO or -CN. Reagent 1: compound of the formula (IV) where R as indicated above; R3 - benzyl. Reagent 2: halogenating agent, preferably sulfuryl chloride. Reagents 1 and 2 after interaction form compound of the formula (V) which is subjected for interaction with ammonia, preferably at the room temperature. Compound of the formula (IV) is synthesized from the compound of the formula (VI) and benzylmercaptan in the medium of aprotonic organic solvent. Synthesized products were used as intermediate compounds for synthesis of pharmaceutically active substances. EFFECT: improved method of synthesis. 6 cl
机译:领域:有机化学。物质:产品-式(I)的6-氟-1,2-苯并异噻唑其中R-氢,低级烷基或式(II)的基团或(III)<图像文件=“ 00000004.GIF” he =“ 18” id =“ imag0.4” imgContent =“ undefined” imgFormat =“ GIF” wi =“ 20 “ />其中R 1 -CHO或-CN。试剂1:式(IV)的化合物其中R如上所示; R 3 -苄基。试剂2:卤化剂,优选为硫酰氯。相互作用后的试剂1和2形成式(V)的化合物最好在室温下与氨相互作用。由式(VI)的化合物合成式(IV)的化合物和苄硫醇在质子惰性有机溶剂的介质中。合成产物用作合成药物活性物质的中间化合物。效果:改进的合成方法。 6厘升

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