从5-甲基脲苷合成司他夫定
被引量:2
Synthesis of stavudine from 5-methyluridine
摘要
目的 研究司他夫定的合成方法。方法 以 5 -甲基脲苷为起始原料 ,经过 5步反应得到目标化合物。结果 目标化合物的结构与文献一致 ,HPLC纯度 99.76 % ,总收率为 5 3.9%。
出处
《西北药学杂志》
CAS
2004年第3期128-129,共2页
Northwest Pharmaceutical Journal
参考文献8
-
1Stefan Becouarn, Stanislas Czernecki and Jean-Marc Valery. Efficient Transformation of Thymidine into 2', 3'-Didehydro-2', 3'-dideoxy-Thymidine (D4T) involving Opening of a 2, 3'-anhydro Derivative by Phenylselenol[J]. Nucleosides & Nucleotides, 1995,14( 被引量:1
-
2Bang-chi Chen, Sandra L, Quinlan, et al. 5'-Benzoyl-2'α- bromo-3'- o-methanesulfonythymidine :A Superior Nucleoside for the Synthesis of the Anti-AIDS Drug D4T (Stavudine) [J]. TetrahedronLetters, 1995, 36(44): 7957-7960. 被引量:1
-
3Hiroshi Shiragami, Takashi Ineyama, Yumiko Uchida and Kunisuke Izawa. Synthesis of 1-(2,3-dideoxy-β-Dglycero-pent-2- enofuranosyl )-Thymine (D4T ; Stavudine ) from 5-Methyluridine [J]. Nucleosides & Nucleotides, 1996,15(1-3) :47-58. 被引量:1
-
4Mansuri MM, Starrett JE, Wos JA, et al. Preparation of 1-( 2, 3-dideoxy-β-D-glycero-pent-2-enofuranosyl )-Thymine (D4T) and 2' 3'-Dideoxyadeosine (DDA) :General Methods for the Synthesis of 2',3'-olefinic and 2',3'-Dideoxy Nucleoside Analogues Active aga 被引量:1
-
5Shiragamai H, Irie Y, Yokozeki K, et al. Synthesis of 2', 3'-dideoxyuridine via deoxygenation of 2', 3'-O-(methoxymethylene) uridine[J]. J Org Chem, 1988,53:5170-5173. 被引量:1
-
6Chu CK, Bhadt VS, Soboszewski B, et al. General Synthesis of 2' , 3'-Dideoxynucleosides and 2', 3'-Didehydro-2' , 3'-Dideoxynucleosides [J]. J Org Chem,1989,54:2217-2225. 被引量:1
-
7Jerome P. Horwitz, Jonathan chua, Margaret A. Da Rooge, et al. Nucleosides. IX. The Formation of 2',3'-Unsaturated Pyrimidine Nucleosides via a Novel β-Elimination Reaction[J]. J Org Chem, 1966,31: 205-211. 被引量:1
-
8Negron G, Islas G, Diaz Y, et al. Quiclet-Sire.Straightforward Synthesis of 1-(2, 3-dideoxy-β-Dglycero-pent-2-enofuranosyl )-Thymine [J].Nucleosides&Nucleotides, 1994,13(4): 1011-1013. 被引量:1
同被引文献22
-
1周婷,谢蓝.HIV非核苷类逆转录酶抑制剂研究进展[J].药学学报,2004,38(8):666-672. 被引量:17
-
2王鲁平,朱永珙.齐多夫定对获得性免疫缺陷综合征的治疗作用和不良反应[J].新药与临床,1996,15(1):38-40. 被引量:9
-
3樊华伟,傅绍军,邵志宇,朱利民.核苷类药物酶法合成研究进展[J].生物技术通讯,2005,16(6):690-692. 被引量:14
-
4De Clercq E.New developments in anti-HIV chemotherapy[J].CurMed Chem,2001,8(13):1543-1572. 被引量:1
-
5Horwitz JR,Chua J,Da Rooge MA,et al.Nucleosides.ⅠⅩ:The formation of 2',3'-unsaturated pyrimidine nucleosides via a novel β-elimination reaction[J].J Org Chem,1966,31(1):205-211. 被引量:1
-
6Mansuri MM,Starrett JE Jr,Ghazzouli I,et al.1-(2,3-Dideoxy-β-D-glycero-pent-2-enofuranosyl) thymine.A highly potent and selective anti-HIV agent[J].J Med Chem,1989,32 (2):461-465. 被引量:1
-
7Mansuri MM,Starrett JE,Wos JA,et al.Preparation of 1-(2,3-dideoxy-β-D-glycero-pent-2-enofuranosyl) thymine(d4T) and 2',3'-dideoxyadenosine (ddA):general methods for the synthesis of 2',3'-olefinic and 2',3'-dideoxy nucleoside analogs active against HIV[J].J Org Chem,1989,54 (20):4780-4785. 被引量:1
-
8Huryn DM,Okabe M.AIDS-driven nucleoside chemistry[J].Chem Rev,1992,92(8):1745-1768. 被引量:1
-
9Luzzio FA,Menes ME.A facile route to pyrimidine-based nucleoside olefins:application to the synthesis of d4T(stavudine)[J].J Org Chem,1994,59 (24):7267-7272. 被引量:1
-
10Paramashivappa R,Phani KP,Subba Rao PV,et al.Simple and efficient method for the synthesis of 2',3',-didehydro-3'-deoxythymidine (d4T)[J].Tetrahedron Lett,2003,44 (5):1003-1005. 被引量:1
二级引证文献3
-
1姜迅知,鞠玻.司他夫定的合成[J].中国医药工业杂志,2007,38(6):403-404. 被引量:1
-
2吴颖,张小红,耿志旺,马玲,乐健,杨永健.RP-HPLC法测定β-司他夫定的有关物质[J].药物分析杂志,2015,35(1):103-108. 被引量:2
-
3陆静,李悦,李春刚.离子色谱法测定齐多夫定原料药中叠氮根的含量[J].分析试验室,2018,37(8):964-967. 被引量:4
-
1陈执中.天然药物抗病毒作用研究进展[J].中国民族民间医药,2003,12(6):311-314. 被引量:8
-
2李丽兰,黎肇炎.蛇毒L-氨基酸氧化酶抗肿瘤作用研究进展[J].蛇志,2006,18(2):127-130. 被引量:5
-
3曹兴午.治疗艾滋病的药物[J].中国性科学,1996,8(4):44-44.
-
4杨泉海,王霞.抗艾滋病病毒药物研究进展[J].首都医药,2004,11(8):41-43. 被引量:9
-
5李珏,李敬云.HIV耐药性研究进展[J].中国艾滋病性病,2004,10(4):309-311. 被引量:10
-
6一种新的安全有效的抗HIV阴道凝胶问世[J].中国艾滋病性病,2008,14(5):500-500.
-
7廖新.英将对两种抗艾滋病病毒霜剂进行大规模人体试验[J].辽宁科技参考,2004(10):43-43.
-
8刘术侠,李白涛,王恩波,曾毅,李泽琳.新型穴状结构阴离子NaSb_9W_(21)O_(86)^(18-)杂多蓝的合成及抗艾滋病病毒(HIV-1)活性[J].科学通报,1997,42(15):1622-1626. 被引量:6
-
9梁馨元.内外药企拉开抗艾药——市场争夺战[J].医药世界,2002(12):25-27.
-
10沈成利,吴昊.抗HIV治疗的副作用(二)——蛋白酶抑制剂[J].中国艾滋病性病,2005,11(4):314-315.