- 英文名称[(2R,3R,4R,5R)-3-Benzoyloxy-5-(2,4-Dioxopyrimidin-1-yl)-4-Fluoro-4-Methyl-Tetrahydrofuran-2-Yl]Methyl Benzoate
- 中文名称索氟布韦 中间体 SF-C2
- IUPAC名称((2R,3R,4R,5R)-3-(benzoyloxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-fluoro-4-methyltetrahydrofuran-2-yl)methyl benzoate
- 其它别名2'Deoxy-2'Fluoro-2'- Methyl- 3'5'-Bis-O- (Phenylcarbonyl) Uridine; ((2R,3R,4R,5R)-3-(Benzoyloxy)-5-(2,4-Dioxo-3,4-Dihydropyrimidin-1(2H)-Yl)-4-Fluoro-4-Methyltetrahydrofuran-2-Yl)Methyl Benzoate; Uridine, 2'-Deoxy-2'-Fluoro-2'-Methyl-, 3',5'-Dibenzoate, (2'R)-; 3',5'-Di-O-Benzoyl-2'-Deoxy-2'-Fluoro-2'-C-Methyluridine; Sofosbuvir Intermediate 3; [(2R,3R,4R,5R)-3-Benzoyloxy-5-(2,4-Dioxopyrimidin-1-Yl)-4-Fluoro-4-Methyl-Tetrahydrofuran-2-Yl]Methyl Benzoate; [(2R,3R,4R,5R)-3-Benzoyloxy-5-(2,4-Dioxopyrimidin-1-Yl)-4-Fluoro-4-Methyl-Tetrahydrofuran-2-Yl; (2R,3R,4R,5R)-2-[(Benzoyloxy)Methyl]-5-(2,4-Dioxo-1,2,3,4-Tetrahydropyrimidin-1-Yl)-4-Fluoro-4-Methyloxolan-3-Yl Benzoate
- CAS编号863329-65-1
- MFCD编号:MFCD27918666
- EINECS号:807-766-2
- 分子式:C24H21FN2O7
- 分子量:468.43
- 产品CID: 1864530
- 产品分类分析化学 → 标准品 → 药典标准品和杂质标准品

欧盟法规
REACH注册ECHA物质上下游产品
(2R,3R,4R,5R)-5-(4-benzamido-2-oxopyrimidin-1(2H)-yl)-2-((benzoyloxy)methyl)-4-fluoro-4-methyltetrahydrofuran-3-yl benzoate ((2R,3R,4R)-3-benzoyloxy-4-fluoro-4-methyl-5-oxo-tetrahydrofuran-2-yl)methyl benzoate (2R,3R,4R,5R)-5-acetoxy-2-((benzoyloxy)methyl)-4-fluoro-4-methyl-tetrahydrofuran-3-yl benzoate ((2R,3R,4S,5R)-3-(benzoyloxy)-5-(2,4-dioxo-3,4-dihydropyrimidin-1(2H)-yl)-4-hydroxy-4-methyltetrahydrofuran-2-yl)methyl benzoate 1-[(2S,3R,4R,5R)-3-fluoro-4-hydroxy-5-hydroxymethyl-3-methyltetrahydrofuran-2-yl]pyrimidine-2,4(1H,3H)-dione (S)-2-{[(2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyltetrahydrofuran-2-ylmethoxy](phenoxy)phosphorylamino}-3-methylbutyric acid methyl ester (S)-2-{(4-bromophenoxy)[(2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyltetrahydrofuran-2-ylmethoxy]phosphorylamino}propionic acid methyl ester (S)-2-{(4-bromophenoxy)-[(2R,3R,4R,5R)-5-(2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-yl)-4-fluoro-3-hydroxy-4-methyltetrahydrofuran-2-ylmethoxy]phosphorylamino}-3-methylbutyric acid methyl ester 合成工艺路线路线简述
- 817204-32-3 = 863329-65-1
反应条件:1.1 Solvents: Acetic Acid; 20 H,Reflux
标题:Synthesis Of Intermediate Of Sofosbuvir
作者:Wang,Zhi-Guo; Et Al
参考文献:Huaxue Shiji 日期:2016 卷标:38(3) 页码:287-290]
1199809-23-8 + 85743-99-3 = 863329-65-1
反应条件:1.1 Reagents: Tin Tetrachloride; 10 H,70 °C; 70 °C -> Rt1.2 Reagents: Sodium Bicarbonate Solvents: Dichloromethane; Rt2.1 Solvents: Acetic Acid; 20 H,Reflux
标题:Synthesis Of Intermediate Of Sofosbuvir
作者:Wang,Zhi-Guo; Et Al
参考文献:Huaxue Shiji 日期:2016 卷标:38(3) 页码:287-290
4-氨基-1-((2R,3R,4R,5R)-3-氟-4-羟基-5-(羟基甲基)-3-甲基四氢呋喃-2-基)嘧啶-2(1H)-酮置于吡啶,溶剂黄146体系中,用 水 作为反应溶剂,化学反应 1.67H,反应生成 索氟布韦 中间体 Sf-C2
参考文献:Nucleoside Phosphoramidate Prodrugs
标题:Nucleoside Phosphoramidate Prodrugs
摘要:本文披露了用于治疗哺乳动物病毒感染的核苷类衍生物的磷酰胺酯前药,该前药是一种化合物,其立体异构体,盐(酸性或碱性加合盐),水合物,溶剂合物或结晶形式,由以下结构表示:同时还披露了治疗方法,用途和制备过程,每种方法均利用由式i表示的化合物.
海关参考信息
- 2905122000-异丙醇
2905310000-1,2-乙二醇
2905320000-1,2-丙二醇
2905399001-1,3-丙二醇 - 💡 提示:海关信息按照顺序优先匹配,如需确认的海关信息,请参考相关资料。
- 详情请参考:📖 海关编码查询和海关进出口税则
专利信息
专利号:US-2011245484-A1
优先权日:2010-03-31
标 题 :Stereoselective synthesis of phosphorus containing actives
专利号:WO-2011123668-A2
优先权日:2010-03-31
标 题:Stereoselective synthesis of phosphorus containing actives
专利号:EP-2752422-B1
优先权日:2010-03-31
标题:Stereoselective synthesis of phosphorus containing actives
专利号:EP-2552931-B1
优先权日:2010-03-31
标题:Stereoselective synthesis of phosphorus containing actives
专利号:US-8859756-B2
优先权日:2010-03-31
标 题 :Stereoselective synthesis of phosphorus containing actives
发明人:ROSS BRUCE S; SOFIA MICHAEL JOSEPH; PAMULAPATI GANAPATI REDDY; RACHAKONDA SUGUNA; ZHANG HAI-REN
权利人:ROSS BRUCE S; SOFIA MICHAEL JOSEPH; PAMULAPATI GANAPATI REDDY; RACHAKONDA SUGUNA; ZHANG HAI-REN; GILEAD PHARMASSET LLC
摘要:Disclosed herein are phosphorus-containing actives, their use as actives for treating diseases, and a stereoselective process for preparing the same. Also disclosed herein are useful synthetic intermediates and processes for preparing the same.