发明名称 Antiviral phosphonate analogs
摘要 The invention is related to phosphorus substituted compounds with antiviral activity, compositions containing such compounds, and therapeutic methods that include the administration of such compounds, as well as to processes and intermediates useful for preparing such compounds.
申请公布号 US8871785(B2) 申请公布日期 2014.10.28
申请号 US201313848593 申请日期 2013.03.21
申请人 Gilead Sciences, Inc. 发明人 Boojamra Constantine G.;Cannizzaro Carina E.;Chen James M.;Chen Xiaowu;Cho Aesop;Chong Lee S.;Fardis Maria;Jin Haolun;Hirschmann Ralph;Huang Alan X.;Kim Choung U.;Kirschberg Thorsten A.;Lee Christopher P.;Lee William A.;Mackman Richard L.;Markevitch David Y.;Oare David A.;Prasad Vidya K.;Pyun Hyung-Jung;Ray Adrian S.;O'Shea Rosemarie;Swaninathan Sundaramoorthi;Watkins William J.;Zhang Jennifer R.
分类号 A61K31/44;C07D239/00 主分类号 A61K31/44
代理机构 Morrison & Foerster LLP 代理人 Morrison & Foerster LLP
主权项 1. A conjugate of the following formula: or a pharmaceutically acceptable salt or solvate thereof; wherein: B is selected from adenine, guanine, cytosine, uracil, thymine, 7-deazaadenine, 7-deazaguanine, 7-deaza-8-azaguanine, 7-deaza-8-azaadenine, inosine, nebularine, nitropyrrole, nitroindole, 2-aminopurine, 2-amino-6-chloropurine, 2,6-diaminopurine, hypoxanthine, pseudouridine, pseudocytosine, pseudoisocytosine, 5-propynylcytosine, isocytosine, isoguanine, 7-deazaguanine, 2-thiopyrimidine, 6-thioguanine, 4-thiothymine, 4-thiouracil, O6-methylguanine, N6-methyladenine, O4-methylthymine, 5,6-dihydrothymine, 5,6-dihydrouracil, 4-methylindole, substituted triazole, and pyrazolo[3,4-d]pyrimidine; X is selected from O, C(Ry)2, OC(Ry)2, NR and S; Z is independently selected from H, OH, OR, NR2, CN, NO2, SH, SR, F, Cl, Br, and I; Y1 is independently O, S, NR, +N(O)(R), N(OR), +N(O)(OR), or N—NR2; Y2 of the moietyis independently CR2, NR, +N(O)(R), N(OR), +N(O)(OR), N—NR2, S, S—S, S(O), or S(O)2; Y2 of the moietyis independently O, CR2, NR, +N(O)(R), N(OR), +N(O)(OR), N—NR2, S, S—S, S(O), or S(O)2; M2 is 0, 1 or 2; Ry is independently H, F, Cl, Br, I, OH, —C(═Y1)R, —C(═Y1)OR, —C(═Y1)N(R)2, —N(R)2, —+N(R)3, —SR, —S(O)R, —S(O)2R, —S(O)(OR), —S(O)2(OR), —OC(═Y1)R, —OC(═Y1)OR, —OC(═Y1)(N(R)2), —SC(═Y1)R, —SC(═Y1)OR, —SC(═Y1)(N(R)2), —N(R)C(═Y1)R, N(R)C(═Y1)OR, or —N(R)C(═Y1)N(R)2, amino (—NH2), ammonium (—NH3+), alkylamino, dialkylamino, trialkylammonium, C1-C8 alkyl, C1-C8 alkylhalide, carboxylate, sulfate, sulfamate, sulfonate, 5-7 membered ring sultam, C1-C8 alkylsulfonate, C1-C8 alkylamino, 4-dialkylaminopyridinium, C1-C8 alkylhydroxyl, C1-C8 alkylthiol, alkylsulfone (—SO2R), arylsulfone (—SO2Ar), arylsulfoxide (—SOAr), arylthio (—SAr), sulfonamide (—SO2NR2), alkylsulfoxide (—SOR), ester (—C(═O)OR), amido (—C(═O)NR2), 5-7 membered ring lactam, 5-7 membered ring lactone, nitrite (—CN), azido (—N3), nitro (—NO2), C1-C8 alkoxy (—OR), C1-C8 alkyl, C1-C8 substituted alkyl, C1-C8 alkenyl, C1-C8 substituted alkenyl, C1-C8 alkynyl, C1-C8 substituted alkynyl, C6-C20 aryl, C6-C20 substituted aryl, C2-C20 heterocycle, C2-C20 substituted heterocycle, polyethyleneoxy, or W3; or when taken together, Ry forms a carbocyclic ring of 3 to 7 carbon atoms; Rx is independently Ry, a protecting group, or the formula: wherein: M1a, M1c, and M1d are independently 0 or 1; M12c is 0, 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11 or 12; and R is C1-C8 alkyl, C1-C8 substituted alkyl, C1-C8 alkenyl, C1-C8 substituted alkenyl, C1-C8 alkynyl, C1-C8 substituted alkynyl, C6-C20 aryl, C6-C20 substituted aryl, C2-C20 heterocycle, C2-C20 substituted heterocycle, or a protecting group; and W3 is W4 or W5, where W4 is R, —C(Y1)Ry, —C(Y1)W5, —SO2Ry, or —SO2W5; and W5 is a carbocycle or a heterocycle wherein W5 is independently substituted with 0 to 3 Ry groups.
地址 Foster City CA US