【药物名称】Mexiletine hydrochloride, Mexitil
化学结构式(Chemical Structure):
参考文献No.345165
标题:Mexiletine
作者:Thorpe, P.; Casta馿r, J.
来源:Drugs Fut 1976,1(4),180
合成路线图解说明:

By hydrogenation of 1-(2',6'-dimethylphenoxy)-2-propanoxime (I) with H2 over Raney-Ni in methanol.

参考文献No.569544
标题:Facile entry to (-)-(R)- and (+)-(S)-mexiletine
作者:Carocci, A.; Franchini, C.; Lentini, G.; Loiodice, F.; Tortorella, V.
来源:Chirality 2000,12(3),103
合成路线图解说明:

The addition reaction of 2,6-dimethylphenol (II) to (S)-2-methyloxirane (I) by means of NaOH in acetonitrile gives (S)-1-(2,6-dimethylphenoxy)-2-propanol (III), which is condensed with phthalimide (IV) by means of DEAD and PPh3 (with inversion of configuration) yielding N-[2-(2,6-dimethylphenoxy)-1(R)-methylethyl]phthalimide (V). Finally, this compound is treated with hydrazine and acetic acid in methanol to eliminate the phthalimido group.

合成路线图解说明:

The addition reaction of 2,6-dimethylphenol (II) to (R)-2-methyloxirane (I) by means of NaOH in acetonitrile gives (R)-1-(2,6-dimethylphenoxy)-2-propanol (III), which is condensed with phthalimide (IV) by means of DEAD and PPh3 (with inversion of configuration) yielding N-[2-(2,6-dimethylphenoxy)-1(S)-methylethyl]phthalimide (V). Finally, this compound is treated with hydrazine and acetic acid in methanol to eliminate the phthalimido group.

参考文献No.701121
标题:
作者:Koeppe, H.; et al.
来源:ZA 6903772
合成路线图解说明:

By hydrogenation of 1-(2',6'-dimethylphenoxy)-2-propanoxime (I) with H2 over Raney-Ni in methanol.

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