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Nýmyndun og hreinsun valasýklóvírs

机译:伐昔洛韦的合成与纯化

摘要

N-tert-Butoxycarbonyl-L-valine-2-[(2-amino-1,6-dihydro-6-oxo-9H-purin-9-yl)methoxy]ethyl ester (I) is new. Independent claims are included for the following: (1) preparation (P1) of (I) comprising coupling N-t-butoxycarbonyl valine with acyclovir in the presence of a coupling agent; (2) preparation (P2) of valacyclovir (II) or its salt involving (a1) coupling an amine protected valine (preferably N-tert-butoxycarbonyl valine (a) or N-formyl valine (b), especially (a)) with acyclovir (c) in the presence of a coupling agent to form a protected valacyclovir, and (a2) deprotecting the protected valacyclovir; (3) preparation (P3) of valacyclovir hydrochloride (III) involving performing step (a1), and deprotecting the protected valacyclovir with hydrochloric acid; and (4) preparation of (III) in pure form involving either: Process A: forming a slurry of (III) in a lower alkyl alcohol (preferably ethanol), refluxing the slurry, and isolating (III) from the slurry; or Process B: forming a solution of (III) in water, mixing the solution with isopropanol to form a slurry, and isolating (III) from the slurry.
机译:N-叔丁氧基羰基-L-缬氨酸-2-[((2-氨基-1,6-二氢-6-氧代-9H-嘌呤-9-基)甲氧基]乙基酯(I)是新的。 (1)(I)的制剂(P1),其包括在偶联剂存在下将N-叔丁氧羰基缬氨酸与阿昔洛韦偶联; (2)伐昔洛韦(II)或其盐的制备(P2),涉及(a1)将胺保护的缬氨酸(最好是N-叔丁氧羰基缬氨酸(a)或N-甲酰基缬氨酸(b),尤其是(a))与阿昔洛韦(c)在偶联剂存在下形成受保护的伐昔洛韦,和(a2)使受保护的伐昔洛韦脱保护; (3)制备盐酸伐昔洛韦(III)的制剂(P3),包括进行步骤(a1),并用盐酸对被保护的伐昔洛韦进行脱保护。 (4)纯净的(Ⅲ)的制备,包括:方法A:在低级烷基醇(最好是乙醇)中形成(Ⅲ)的淤浆,使淤浆回流,并从淤浆中分离(Ⅲ)。或方法B:形成(III)在水中的溶液,将该溶液与异丙醇混合以形成淤浆,并从该淤浆中分离(III)。

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