新产品编号:1365775
Chemical Name: (6R,8R,9R)-N-[4-Amino-9-(tert-butyldimethylsilyloxy)-6-(tert-butyldimethylsilyloxymethyl)-1,7-dioxa-2-thiaspiro[4.4]-3-nonen-8-yl]-N'-(2-methylpropenoyl)urea S,S-dioxide
项目整合开发状态: Biological Testing
项目研究机构: CSIC (Originator), Rega Institute for Medical Research (Originator)
合成路线:The reduction of azide (I) with trimethylphosphine in THF gives the amine (II),which is then treated with methacryloyl isocyanate (III) in acetonitrile yielding a mixture of alpha and beta phenylureas which is separated by centrifugal circular thin layer chromatography.
合成路线:The reduction of azide (I) with trimethylphosphine in THF gives the amine (II),which is treated with chlorosulfonyl isocyanate (A) in acetonitrile yielding the urea derivative (III).Finally,this compound is acetylated with acetic anhydride in pyridine to afford a mixture of alpha and beta acetylureas which is separated by centrifugal circular thin layer chromatography.
合成路线:The reduction of azide (I) with trimethylphosphine in THF gives the amine (II),which is then treated with phenyl isocyanate (A) in acetonitrile yielding a mixture of alpha and beta phenylureas which is separated by centrifugal circular thin layer chromatography.
📌 参考资料/链接:
参考文献标题:Abasic analogues of TSAO-T as the first sugar derivatives that specifically inhibit HIV-1 reverse transcriptase
文献作者:Vel醶quez,S.; Chamorro,C.; Perez-Perez,M.J.; Alvarez,R.; Jimeno,M.L.; Martin-Domenech,A.; Perez,C.; Gago,F.; De Clercq,E.; Balzarini,J.; San-Felix,A.; Camarasa,M.J.
参考来源:J Med Chem 1998,41(23),4636