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Synthesis and Reactivity in [3+2] Cycloadditions of Isoxanthopterin N(5)-Oxides – A New Synthesis of 6-Substituted Pteridinediones
Helvetica Chimica Acta ( IF 1.5 ) Pub Date : 29 OCT 2008 , DOI: 10.1002/hlca.200890201
Thomas Steinlin , Tiziana Sonati , Andrea Vasella

Intramolecular condensation of the N-(4-amino-5-nitrosopyrimidin-4-yl)-2-chloroacetamide 2 led to the pteridinone N(5)-oxide 4, while treatment of 2 with Me3P yielded the 8-(chloromethyl)purine 3. A high-yielding [3+2] dipolar cycloaddition of the N(5)-oxide 4 to electron-poor dipolarophiles, followed by spontaneous N,O-bond cleavage, gave the C(6)-substituted pteridinones 8a8d that were deprotected to provide the pteridine-4,7(3H,8H)-diones 9a9d, constituting a new synthesis of pterinones possessing a functionalised side chain at C(6).

中文翻译:

异黄蝶呤N(5) -氧化物的[3 + 2]环加成反应中的合成和反应性-6-取代的蝶啶二酮的新合成

所述的分子内缩合ñ - (4-氨基-5-亚硝基嘧啶-4-基)-2-氯乙酰胺2导致了蝶啶酮N(5) -氧化物4,而治疗的2与我3 P,得到8-(氯甲基嘌呤3N(5)-氧化物4向电子贫乏的偶极亲和物的高产率[3 + 2]偶极环加成反应,然后自发进行N,O键裂解,得到C(6)取代的蝶啶8a8d,它们分别是去保护得到蝶啶-4,7 (3 H,8 H)-二酮9a参见图9d,其构成在C(6)处具有官能化侧链的蝶呤的新合成。
更新日期:2017-01-31
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