Spiropentane mimics of nucleosides:: Analogues of 2′-deoxyadenosine and 2′-deoxyguanosine.: Synthesis of all stereoisomers, isomeric assignment, and biological activity

被引:45
|
作者
Guan, HP
Ksebati, MB
Cheng, YC
Drach, JC
Kern, ER
Zemlicka, J
机构
[1] Wayne State Univ, Sch Med, Barbara Ann Karmanos Canc Inst, Dept Chem,Expt & Clin Chemotherapy Program, Detroit, MI 48201 USA
[2] Wayne State Univ, Dept Chem, Cent Instrumentat Facil, Detroit, MI 48202 USA
[3] Yale Univ, Sch Med, Dept Pharmacol, New Haven, CT 06510 USA
[4] Univ Michigan, Sch Dent, Dept Biol & Mat Sci, Ann Arbor, MI 48019 USA
[5] Univ Alabama, Dept Pediat, Birmingham, AL 35294 USA
来源
JOURNAL OF ORGANIC CHEMISTRY | 2000年 / 65卷 / 05期
关键词
D O I
10.1021/jo991030r
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Synthesis of spirocyclic analogues of 2'-deoxyadenosine and 2'-deoxyguanosine (12a-15a and 12b-15b) is described. Rhodium-catalyzed reaction of ethyl diazoacetate with methylenecyclopropane 19, obtained from 2-bromo-2-bromomethylcyclopropane 17 via debromination (18), reduction (18), and acetylation (19), gave a mixture of all four isomeric spiropentanes 20a-20d. Hydrolysis afforded hydroxy carboxylic acids 21a-21d. Acetylation of separated proximal + medial-syn isomers 21a + 21b and medial anti + distal isomers 21c + 21d furnished acetates 22a + 22b and 22c + 22d. Curtius rearrangement effected by diphenylphosphoryl azide in tert-butyl alcohol performed separately with mixtures 22a + 22b and 22c + 22d led to BOC-amino spiropentanes 23a + 23b and 23c + 23d. After deacetylation all isomers 24a-24d were separated and deprotected to give aminospiropentane hydrochlorides 25a-25d. Free bases were of limited stability, The heterocyclic moieties were introduced into individual isomers 25a-25d via 6-chloropurine derivatives 26a-26d or 30a-30d. Ammonolysis of 26a-26d furnished the adenine isomeric series 12a-15a, whereas guanine derivatives 12b-15b were obtained by hydrolysis of 30a-30d with formic acid. The isomeric assignments followed fi om IR spectra of BOC-aminospiropentanes 24a-24d and NMR spectra of 12a-15a including NOE and (H,H) COSY. The proximal and medial-syn isomers 12a and 12b were modest inhibitors of human cytomegalovirus (HCMV) and Epstein-Barr virus (EBV) in culture, whereas the medial-anti isomer 12c was a substrate for adenosine deaminase. The distal isomer 15b was an anti-EBV agent. The medial-syn phosphoralaninate 34 was an effective;re inhibitor of HCMV replication in vitro. It tvas also active against herpes simplex virus type I. (HSV-1), varicella tester virus (VZV), human immunodeficiency virus (HN-I), hepatitis B virus (HBV), and EBV with a varying degree of cytotoxicity.
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收藏
页码:1280 / 1290
页数:11
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