首页> 外国专利> (A) Process: A=R4-phenyl or pyridyl; R1 and R2=H, halogen, CF3 or nitro; R3=H or low alkyl; R4=H or halogen; L=a group which can be split off such as a ha

(A) Process: A=R4-phenyl or pyridyl; R1 and R2=H, halogen, CF3 or nitro; R3=H or low alkyl; R4=H or halogen; L=a group which can be split off such as a ha

机译:(A)方法:A = R4-苯基或吡啶基; R1和R2 = H,卤素,CF3或硝基; R3 = H或低级烷基; R4 = H或卤素; L =一个可以分开的基团,例如ha

摘要

(A) Process: A=R4-phenyl or pyridyl; R1 and R2=H, halogen, CF3 or nitro; R3=H or low alkyl; R4=H or halogen; L=a group which can be split off such as a halogen atom or a sulphonyloxy group. (B) Compounds of formula (II) where A= a 6-pyridyl group pref. connected with the benzoxadiazocine nucleus at the 2-pos of the pyridyl group; R2=preferably H; R1=preferably halogen such as Cl or Br at the 8-pos. of the benzoxadiazocine nucleus. Compounds (II) are important intermediates in the synthesis of compounds with sedative, muscle-relaxant and anti-convulsive properties. The 1,3-dihydro 6-pyridyl 2H-4, 1,5-benzoxadiazocine 2-ones have also sedative-, muscle relaxant and anti-convulsive properties. The new process is simple and gives good yields. Compounds (III) where A=pyridyl can be easily synthesised from easily obtainable starting materials.
机译:(A)方法:A = R4-苯基或吡啶基; R1和R2 = H,卤素,CF3或硝基; R3 = H或低级烷基; R4 = H或卤素; L =可以分裂的基团,例如卤素原子或磺酰氧基。 (B)其中A = 6-吡啶基优选的式(II)化合物。在吡啶基的2-位与苯并恶二唑嗪核连接; R2 =优选H; R1 =优选在8位上的卤素如Cl或Br。苯并恶二唑啉核。化合物(II)是合成具有镇静,舒缓肌肉和抗惊厥特性的化合物的重要中间体。 1,3-二氢6-吡啶基2H-4、1,5-苯并恶二唑啉2-酮还具有镇静,肌肉松弛和抗惊厥作用。新工艺简单,产量高。 A =吡啶基的化合物(III)可以容易地从容易获得的起始原料合成。

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