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SYNTHESIS OF OPTICALLY ACTIVE LACTONES FORM L-ASPARTIC ACID AND INTERMEDIATES THEREOF

机译:光学活性内酯从L-天冬氨酸的合成及其中间体

摘要

2110572 9221675 PCTABS00017 Optically active lactones are described, such as an intermediate lactone having formula (VIa) where R and R2 are each independently alkyl with 1 to 6 carbon atoms, cycloalkyl with 6 to 10 carbon atoms, aryl with 6 to 10 carbon atoms, or arylalkyl with 7 to 19 carbon atoms, R4 is H or C1-6 alkyl, and Ar is a homo- or heteroaromatic ring with 5 or 6 ring atoms being optionally substituted by C1-6 alkyl or alkoxy groups, halogen atoms, cyano or nitro groups. Such optically active, intermediate lactones are prepared from L-aspartic acid, and can be readily converted to (+)-pilocarpine and its analogues by hydrolysis, reduction, and hydrogenation, such as to an optically active lactone having formula (VIII) which is (+)-pilocarpine when R is ethyl, R4 is H, and Ar is 1-methylimidazol-5-yl.
机译:2110572 9221675 PCTABS00017描述了旋光内酯,例如具有式(VIa)的中间体内酯,其中R和R2各自独立地为具有1至6个碳原子的烷基,具有6至10个碳原子的环烷基,具有6至10个碳原子的芳基,或具有7至19个碳原子的芳烷基,R4为H或C1-6烷基,且Ar为具有5或6个环原子的可被C1-6烷基或烷氧基,卤素原子,氰基或硝基。此类旋光的中间体内酯由L-天冬氨酸制备,并且可以通过水解,还原和氢化容易地转化为(+)-毛果芸香碱及其类似物,例如具有式(VIII)的旋光内酯。当R为乙基,R4为H,且Ar为1-甲基咪唑-5-基时,(+)-哌咯烷。

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