PROCESS FOR THE PREPARATION OF AN OXIRANE, AZIRIDINE OR CYCLOPROPANE
    1.
    发明公开
    PROCESS FOR THE PREPARATION OF AN OXIRANE, AZIRIDINE OR CYCLOPROPANE 失效
    用于生产环氧乙烷,氮丙啶和环丙烷

    公开(公告)号:EP0983236A2

    公开(公告)日:2000-03-08

    申请号:EP98919377.6

    申请日:1998-05-01

    摘要: A process for the preparation of an oxirane, aziridine or cyclopropane of formula (I) wherein X is oxygen, NR?4 or CHR5; R1¿ is hydrogen, alkyl, aryl, heteroaromatic, heterocyclic or cycloalkyl; R2 is hydrogen, alkyl, aryl, heteroaromatic, CO¿2?R?8, CHR14NHR13¿, heterocyclic or cycloalkyl; or R?1 and R2¿ join together to form a cycloalkyl ring; R?3 and R10¿ are, independently, hydrogen, alkyl, aryl, heteroaromatic, CO¿2R?8, R83Sn, CONR8R9, trialkylsilyl or triarylsilyl; R4 is an electron withdrawing group; R5 is alkyl, cycloalkyl, aryl, heteroaromatic, SO¿2R?8, SO3R?8, COR8, CO¿2R?8, CONR8R9, PO(R8)¿2, PO(OR8)2 or CN; R?8 and R9¿ are independently alkyl or aryl; and R?13 and R14¿ are independently hydrogen, alkyl or aryl is provided. The process comprises degrading a compound of the formula (II), (IIa), (IIb) or (IIc), wherein R?3 and R10¿ are as defined above; Y is a cation; depending on the nature of Y, r is 1 or 2; and L is a suitable leaving group, to form a diazo compound. The diazo compound is reacted with a suitable transition metal catalyst, and the product thereof reacted with a sulphide of the formula SR6R7, wherein R?6 and R7¿ are independently alkyl, aryl or heteroaromatic, or R?6 and R7¿ join together to form an optionally substituted ring which optionally includes an additional heteroatom. This product is then reacted with an aldehyde, ketone, imine or alkene.

    PROCESS FOR THE PREPARATION OF AN OXIRANE, AZIRIDINE OR CYCLOPROPANE
    3.
    发明授权
    PROCESS FOR THE PREPARATION OF AN OXIRANE, AZIRIDINE OR CYCLOPROPANE 失效
    用于生产环氧乙烷,氮丙啶和环丙烷

    公开(公告)号:EP0983236B1

    公开(公告)日:2003-09-10

    申请号:EP98919377.6

    申请日:1998-05-01

    摘要: A process for the preparation of an oxirane, aziridine or cyclopropane of formula (I) wherein X is oxygen, NR?4 or CHR5; R1¿ is hydrogen, alkyl, aryl, heteroaromatic, heterocyclic or cycloalkyl; R2 is hydrogen, alkyl, aryl, heteroaromatic, CO¿2?R?8, CHR14NHR13¿, heterocyclic or cycloalkyl; or R?1 and R2¿ join together to form a cycloalkyl ring; R?3 and R10¿ are, independently, hydrogen, alkyl, aryl, heteroaromatic, CO¿2R?8, R83Sn, CONR8R9, trialkylsilyl or triarylsilyl; R4 is an electron withdrawing group; R5 is alkyl, cycloalkyl, aryl, heteroaromatic, SO¿2R?8, SO3R?8, COR8, CO¿2R?8, CONR8R9, PO(R8)¿2, PO(OR8)2 or CN; R?8 and R9¿ are independently alkyl or aryl; and R?13 and R14¿ are independently hydrogen, alkyl or aryl is provided. The process comprises degrading a compound of the formula (II), (IIa), (IIb) or (IIc), wherein R?3 and R10¿ are as defined above; Y is a cation; depending on the nature of Y, r is 1 or 2; and L is a suitable leaving group, to form a diazo compound. The diazo compound is reacted with a suitable transition metal catalyst, and the product thereof reacted with a sulphide of the formula SR6R7, wherein R?6 and R7¿ are independently alkyl, aryl or heteroaromatic, or R?6 and R7¿ join together to form an optionally substituted ring which optionally includes an additional heteroatom. This product is then reacted with an aldehyde, ketone, imine or alkene.