(S)-P-neopentyl 2-((S)-(((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphorylamino)propanoate | 1234490-84-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (S)-P-neopentyl 2-((S)-(((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphorylamino)propanoate
• 英文别名: (S)-neopentyl 2-(((S)-(((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphoryl)amino)propanoate；(2S)-neopentyl-2-(((((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphoryl)amino)propanoate；neopentyl ((((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphoryl)-L-alaninate；INX10005；(S)-P 2,2-dimethylpropyl (2S)-2-((((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalene-1-yloxy)phosphorylamino)propanoate；2,2-Dimethylpropyl (2S)-2-{[{[(2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl]methoxy}(naphthalen-1-yloxy)phosphoryl]amino}propanoate；2,2-dimethylpropyl (2S)-2-[[[(2R,3R,4R,5R)-5-(2-amino-6-methoxypurin-9-yl)-3,4-dihydroxy-4-methyloxolan-2-yl]methoxy-naphthalen-1-yloxyphosphoryl]amino]propanoate
• CAS: 1234490-84-6
• 化学式: C₃₀H₃₉N₆O₉P
• 分子量: 658.648
• InChiKey: YFXGICNMLCGLHJ-KGSOWIGMSA-N

物化性质

• 沸点：
  848.7±75.0 °C(Predicted)
• 密度：
  1.47±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  46
• 可旋转键数：
  13
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.47
• 拓扑面积：
  202
• 氢给体数：
  4
• 氢受体数：
  14

反应信息

• 作为产物：
  描述：

  N-(2'-C-甲基-6-O-甲基-P-1-萘基-5'-鸟苷酰基)-L-丙氨酸 2,2-二甲基丙酯 在 Chiral Pak AD 作用下， 以 hexanes 、 乙醇 为溶剂， 以95.9%的产率得到(S)-P-neopentyl 2-((S)-(((2R,3R,4R,5R)-5-(2-amino-6-methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen-1-yloxy)phosphorylamino)propanoate
  参考文献：
  名称：

  [EN] PHOSPHORAMIDATE DERIVATIVES OF GUANOSINE NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS
  [FR] DÉRIVÉS DE PHOSPHORAMIDATE DE COMPOSÉS GUANOSINE NUCLÉOSIDE POUR LE TRAITEMENT D'INFECTIONS VIRALES

  摘要：

  公开号：

  WO2010081082A3

文献信息

• PHOSPHORIC ACID/PHOSPHONIC ACID DERIVATIVES AND MEDICINAL USES THEREOF
  申请人：BEIJING MEIBEITA DRUG RES CO., LTD.

  公开号：US20160115186A1

  公开（公告）日：2016-04-28

  The present invention relates to phosphoric acid/phosphonic acid derivatives shown by formula (I), wherein, R 1 or R 2 represents the following structures: (Q1), or (Q2), or (Q3). Q1 represents ester derivatives of L-amino acid, wherein R 3 is alkyl with 1-6 carbon atoms or cycloalkyl, R 4 is H or alkyl with 1-6 carbon atoms; Q2 represents hydroxyl substituted benzodioxane derivatives; Q3 represents hydroxyl substituted benzodioxolane derivatives; R 1 or R 2 is the same or different, but at least one of them is Q2 or Q3; D represents residues of pharmacologically active molecules containing a phosphate/phosphonate group, i.e. formula (II) represents pharmacologically active molecules containing a phosphate/phosphonate group; and when R 1 and R 2 are different, the configuration of the P atom connected to R 1 and R 2 is of R or S type.

  本发明涉及由式（I）所示的磷酸/膦酸衍生物，其中，R1或R2代表以下结构：（Q1），或（Q2），或（Q3）。Q1代表L-氨基酸的酯衍生物，其中R3是具有1-6个碳原子的烷基或环烷基，R4是H或具有1-6个碳原子的烷基；Q2代表羟基取代的苯二噁烷衍生物；Q3代表羟基取代的苯二噁唑烷衍生物；R1或R2相同或不同，但它们中至少有一个是Q2或Q3；D代表含有磷酸/膦酸基团的药理活性分子的残基，即式（II）代表含有磷酸/膦酸基团的药理活性分子；当R1和R2不同时，连接到R1和R2的P原子的构型为R型或S型。
• [EN] CRYSTALLINE SOLVATES OF NUCLEOSIDE PHOSPHOROAMIDATES, THEIR STEREOSELECTIVE PREPARATION, NOVEL INTERMEDIATES THEREOF, AND THEIR USE IN THE TREATMENT OF VIRAL DISEASE<br/>[FR] SOLVATES CRISTALLINS DE NUCLÉOSIDE PHOSPHOROAMIDATES, LEUR PRÉPARATION STÉRÉOSÉLECTIVE, NOUVEAUX INTERMÉDIAIRES DE CEUX-CI ET LEUR UTILISATION DANS LE TRAITEMENT D'UNE MALADIE VIRALE
  申请人：INHIBITEX INC

  公开号：WO2013066991A1

  公开（公告）日：2013-05-10

  This invention is directed to novel crystalline solvates of the (S)-P diastereomer of the anti- HCV nucleoside phosphoroamidate, (2S)-neopentyl 2-((((2R,3R,4R,5R)-5-(2-amino-6- methoxy-9H-purin-9-yl)-3,4-dihydroxy-4-methyltetrahydrofuran-2-yl)methoxy)(naphthalen- l-yloxy)phosphorylamino)propanoate (also referred to as INX-08189 or IΝΧ-189), and to a recrystallization method for separating the two diastereomers of INX-08189. In addition, this application relates to a novel stereoselective method for the preparation of either of the two diastereomers, and to the novel synthetic intermediates used in this stereoselective synthesis. The invention also relates to the use of the crystalline solvates to increase the liver exposure of 2'-C-methyl guanosine triphosphate from an oral dose.

  该发明涉及抗HCV核苷磷酸酰胺的(S)-P对映体的新型晶体溶剂化合物，(2S)-新戊基2-((((2R,3R,4R,5R)-5-(2-氨基-6-甲氧基-9H-嘌呤-9-基)-3,4-二羟基-4-甲基四氢呋喃-2-基)甲氧基)(萘基氧基)磷酰胺)丙酸酯（也称为INX-08189或INX-189），以及用于分离INX-08189两个对映体的重结晶方法。此外，该申请涉及一种新颖的立体选择性制备两个对映体的方法，以及用于这种立体选择性合成的新型合成中间体。该发明还涉及利用晶体溶剂化合物提高2'-C-甲基鸟苷三磷酸酯从口服剂量中的肝脏暴露。
• [EN] PROCESS FOR PREPARING PHOSPHORAMIDATE DERIVATIVES OF NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS<br/>[FR] PROCÉDÉ DE PRÉPARATION DE DÉRIVÉS PHOSPHORAMIDATÉS DE COMPOSÉS NUCLÉOSIDIQUES UTILISABLES EN VUE DU TRAITEMENT D'INFECTIONS VIRALES
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2014047117A1

  公开（公告）日：2014-03-27

  Processes for the production of nucleoside phosphoramidate compounds having the following Formula I are provided.

  提供生产以下化学式I的核苷酸磷酰胺化合物的工艺。
• [EN] PROCESS FOR PREPARING DIASTEREOMERICALLY ENRICHED PHOSPHORAMIDATE DERIVATIVES OF NUCLEOSIDE COMPOUNDS FOR TREATMENT OF VIRAL INFECTIONS<br/>[FR] PROCÉDÉ DE PRÉPARATION DE DÉRIVÉS DE PHOSPHORAMIDATES ENRICHIS EN DIASTÉRÉO-ISOMÈRES DE COMPOSÉS DE NUCLÉOSIDES, DESTINÉS AU TRAITEMENT D'INFECTIONS VIRALES
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2014008236A1

  公开（公告）日：2014-01-09

  The present invention is directed to a process for preparing diastereomerically enriched nucleoside phosphoramidates having the formula I:

  本发明涉及一种制备具有化学式I的对映异构体富集的核苷磷酰胺酯的方法。
• Diastereoselective synthesis of P-chirogenic phosphoramidate prodrugs of nucleoside analogues (ProTides) via copper catalysed reaction
  作者：F. Pertusati、C. McGuigan

  DOI：10.1039/c5cc00448a

  日期：——

  The first example of transition metal assisted diastereoselective synthesis of phosphoramidate of nucleoside analogues is presented.

  第一个过渡金属辅助的立体选择性合成核苷酸类似物的磷酰胺酰化物的例子被提出。