4931-66-2 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol 标题:Synthesis Of New Optically Active 2-Pyrrolidinones 作者:Moutevelis-Minakakis,Panagiota; Papavassilopoulou,Eleni; Mavromoustakos,Thomas 参考文献:Molecules 日期:2013 卷标:18 页码:50-73]
7149-65-7 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol 标题:Approaches Towards The Synthesis Of Ebelactone-A Using Organosilicon Chemistry 作者:Archibald,Sarah Catherine 参考文献:1992]
4931-66-2 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol 标题:Synthesis,In Silico Docking Experiments Of New 2-Pyrrolidinone Derivatives And Study Of Their Anti-Inflammatory Activity 作者:Moutevelis-Minakakis,Panagiota; Papavassilopoulou,Eleni; Michas,George; Georgikopoulou,Kalliopi; Ragoussi,Maria-Eleni; Et Al 参考文献:Bioorganic & Medicinal Chemistry 日期:2011 卷标:19(9) 页码:2888-2902]
7149-65-7 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol 标题:An Approach To The Synthesis Of Nonactic Acid 作者:Duyck,Catherine 参考文献:1991]
4931-66-2 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol,Water 标题:Synthesis Of Novel Heterocyclic Compounds As Potential Pharmaceuticals 作者:Bhattacharya,Kaberi 参考文献:1991]
7149-65-7 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Ethanol 标题:Stereoselective Synthesis And Evaluation Of All Stereoisomers Of Z4349,A Novel And Selective μ-Opioid Analgesic 作者:Napoletano,M.; Della Bella,D.; Fraire,C.; Grancini,G.; Masotto,C.; Et Al 参考文献:Bioorganic & Medicinal Chemistry Letters 日期:1995 卷标:5(6) 页码:589-92]
7149-65-7 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol 标题:The Stereochemistry Of Electrophilic Attack On Chiral Dienylmethylsilanes 作者:Jones,Graeme Robert 参考文献:1992]
7149-65-7 = 17342-08-4 反应条件:1.1 Reagents: Sodium Borohydride Solvents: Methanol 标题:Studies Directed Towards The Synthesis Of (-)-Ebelactone A 作者:Mandal,Ajay K. 参考文献:1999]
98-79-3 = 17342-08-4 反应条件:1.1 Reagents: Methanol,Thionyl Chloride Solvents: Methanol; Rt1.2 Reagents: Sodium Borohydride Solvents: Ethanol; Rt 标题:First Total Synthesis Of Oteromycin Utilizing One-Pot Four-Step Cascade Reaction Strategy 作者:Uchiro,Hiromi; Shionozaki,Nobuhiro; Tanaka,Ryo; Kitano,Hiroyuki; Iwamura,Naoki; Et Al 参考文献:Tetrahedron Letters 日期:2013 卷标:54(6) 页码:506-511
专利号:US-2025066296-A1 优先权日:2021-12-14 标题 :Methods for the synthesis of complement factor d inhibitors and intermediates thereof 发明人:HASHIMOTO AKIHIRO; PHADKE AVINASH; RAI U SANKAPPA; CHANDRAN PRABU 权利人:ALEXION PHARMA INC 摘要:The present disclosure provides methods for the synthesis of complement factor D inhibitors and intermediates thereof.
专利号:US-8143416-B2 优先权日:2004-08-31 标题 :Alternative synthesis of renin inhibitors and intermediates thereof 发明人:SEDELMEIER GOTTFRIED; MICKEL STUART JOHN; RUEEGER HEINRICH 权利人:SEDELMEIER GOTTFRIED; MICKEL STUART JOHN; RUEEGER HEINRICH; NOVARTIS AG 摘要:The present invention relates to synthetic routes to prepare a compound of the formula n nwherein R 1 is halogen, C 1-6 halogenalkyl, C 1-6 alkoxy-C 1-6 alkyloxy or C 1-6 alkoxy-C 1-6 alkyl; R 2 is halogen, C 1-4 alkyl or C 1-4 alkoxy; R 3 and R 4 are independently branched C 3-6 alkyl; and R 5 is cycloalkyl, C 1-6 alkyl, C 1-6 hydroxyalkyl, C 1-6 alkoxy-C 1-6 alkyl, C 1-6 alkanoyloxy-C 1-6 alkyl, C 1-6 aminoalkyl, C 1-6 alkylamino-C 1-6 alkyl, C 1-6 dialkylamino-C 1-6 alkyl, C 1-6 alkanoylamino-C 1-6 alkyl, HO(O)C—C 1-6 alkyl, C 1-6 alkyl-O—(O)C—C 1-6 alkyl, H 2 N—C(O)—C 1-6 alkyl, C 1-6 alkyl-HN—C(O)—C 1-6 alkyl or (C 1-6 alkyl) 2 N—C(O)—C 1-6 alkyl; or a pharmaceutically acceptable salt thereof as well as key intermediates obtained when following these routes as well as their preparation.
专利号:US-8921573-B2 优先权日:2011-10-18 标 题:Processes for the preparation of novel benzimidazole derivatives 发明人:TANG DATONG; XU GUOYOU; PENG XIAOWEN; YING LU; WANG CE; CAO HUI; LONG JIANG; KIM IN JONG; WANG GUOQIANG; QIU YAO-LING; OR YAT SUN 权利人:ENANTA PHARM INC 摘要:The present invention relates to processes and intermediates for the preparation of novel benzimidazole derivatives, especially in the synthesis of hepatitis C virus NS5A inhibitors. In particular, the present invention relates to processes and intermediates for the preparation of compounds of formulae (I-a):
专利号:WO-2023114200-A2 优先权日:2021-12-14 标题 :Methods for the synthesis of complement factor d inhibitors and intermediates thereof
专利号:US-6949553-B2 优先权日:2001-06-18 标题 :Aliphatic compounds, their synthesis method, and utilization of the same 发明人:TAMAI TADAKAZU; YOSHIKAI KAZUYOSHI; NISHIKAWA MASAZUMI; OGASAWARA KUNIO; MUROTA ITSUKI 权利人:MARUHA CORP 摘要:The present invention relates to aliphatic compounds of the formula I, or stereoisomers thereof, or their pharmaceutically acceptable salts: n n nwherein A represents an optionally substituted CH 3 C n H (2n-2m) — (wherein n denotes an integer of 4 to 22, and m represents an unsaturation number which is an integer of 0 to 7), l represents an integer of 0 to 10, s represents 0 or 1, provided that when s is 0, p+q=4 or 5, but when s is 1, p+q=3 or 4, and in each case, either p or q is an integer of 1 or more, R represents an alkyl group having 1 to 10 carbon atoms which may be straight-chain or branched-chain, and R A represents hydrogen or an alkyl group having 1 to 10 carbon atoms which may be straight-chain or branched-chain, and their use in suppression of platelet aggregation, in suppression of inflammation, and in prevention and treatment of circulatory diseases.
专利号:US-2007208055-A1 优先权日:2004-08-31 标题 :Alternative synthesis of renin inhibitors and intermediates thereof