thiazol-4-ylmethyl (+/-)-3-[4-(1-methyl-1-phenyl-ethyl)phenoxymethyl]pyrrolidine-1-carboxylate | 1315546-44-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: thiazol-4-ylmethyl (+/-)-3-[4-(1-methyl-1-phenyl-ethyl)phenoxymethyl]pyrrolidine-1-carboxylate
• 英文别名: 1,3-Thiazol-4-ylmethyl 3-[[4-(2-phenylpropan-2-yl)phenoxy]methyl]pyrrolidine-1-carboxylate
• CAS: 1315546-44-1
• 化学式: C₂₅H₂₈N₂O₃S
• 分子量: 436.575
• InChiKey: NWWYCXUJBDIYSK-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  5.5
• 重原子数：
  31
• 可旋转键数：
  8
• 环数：
  4.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  79.9
• 氢给体数：
  0
• 氢受体数：
  5

文献信息

• [EN] ALKYL-HETEROCYCLE CARBAMATE DERIVATIVES, THEIR PREPARATION AND THEIR THERAPEUTIC APPLICATION<br/>[FR] DÉRIVÉS CARBAMATES ALKYL-HÉTÉROCYCLIQUES, LEUR PRÉPARATION ET LEUR APPLICATION THÉRAPEUTIQUE
  申请人：SANOFI AVENTIS

  公开号：WO2011089550A1

  公开（公告）日：2011-07-28

  The invention relates to compounds corresponding to the general formula (I) : in which R2 represents a hydrogen, fluorine, hydroxyl, cyano, trifluoromethyl, C1-6-alkyl, C1-6-alkoxy or -NR8R9; n and m represent, independently of one another, an integer equal to 1, 2 or 3, it being understood that the sum m+n is at most equal to 5; A represents a covalent bond, an oxygen, a C1-6-alkylene or -O-C1-6-alkylene; R1 represents a phenyl or a heterocycle which is optionally substituted; R3 represents a hydrogen, fluorine, C1-6-alkyl or trifluoromethyl; R4 represents an optionally substituted 5-membered heterocycle; in the form of the base or of an addition salt with an acid; with the exclusion of 5-methylisoxazol-3-ylmethyl 4-hydroxy-4- (4- chlorophenyl) piperidine-1-carboxylate. The invention also relates to a process for the preparation of the compounds of formula (I), to compositions comprising them and to their therapeutic application.

  本发明涉及与通式（I）相对应的化合物： 其中，R2表示氢、氟、羟基、氰基、三氟甲基、C1-6烷基、C1-6烷氧基或-NR8R9；n和m分别表示等于1、2或3的整数，其中m+n的总和最多等于5；A表示共价键、氧、C1-6-烷基亚甲基或-O-C1-6-烷基亚甲基；R1表示苯基或可选取代的杂环；R3表示氢、氟、C1-6烷基或三氟甲基；R4表示可选取代的5-成员杂环；以碱或酸的加成盐的形式存在。 本发明还涉及制备通式（I）化合物的方法、包含它们的组合物以及它们的治疗应用，但不包括5-甲基异噁唑-3-基甲基4-羟基-4-（4-氯苯基）哌啶-1-羧酸酯。
• TRICYCLIC OXAZOLIDINONE ANTIBIOTIC COMPOUNDS
  申请人：Hubschwerlen Christian

  公开号：US20110195961A1

  公开（公告）日：2011-08-11

  The invention relates to antibacterial compounds of formula I wherein is a bond or is absent, V is CH, CR 6 or N; R 0 is H or, if is a bond, may also be alkoxy; R 1 is notably H or halogen; U is CH or N when is a bond, or, if is absent, U is CH 2 , NH or NR 9 ; R 2 is H, alkylcarbonyl or —CH 2 —R 3 ; R 3 is H, alkyl or hydroxyalkyl; R 4 is H or, if n is not 0 and R 5 is H, may also be OH; R 5 is H, alkyl, hydroxyalkyl, aminoalkyl, alkoxyalkyl, carboxy or alkoxycarbonyl; R 6 is hydroxyalkyl, carboxy, alkoxycarbonyl or —(CH 2 ) q —NR 7 R 8 , q being 1, 2 or 3 and each of R 7 and R 8 independently being H or alkyl or R 7 and R 8 forming with the N atom bearing them a ring; R 9 is alkyl or hydroxyalkyl; A is —(CH 2 ) p —, —CH 2 CH 2 CH(OH)— or —COCH 2 CH(OH)—; G is substituted phenyl or G 1 or G 2 wherein Q is O or S and X is CH or N; and Y 1 , Y 2 and Y 3 may each be CH or N; and n is 0 when A is —CH 2 CH 2 CH(OH)— or —COCH 2 CH(OH)—, and n is 0, 1 or 2 when A is —(CH 2 ) p —, p being 1, 2, 3 or 4, with the proviso that the sum of n and p is then 2, 3 or 4; and to salts of such compounds.

  该发明涉及式I的抗菌化合物，其中： - 当V为CH或N时，U为CH或N，R1为H或卤素，R2为H、烷基羰基或—CH2—R3，R3为H或烷基羟基，R4为H或OH（当n不为0且R5为H时），R5为H、烷基、羟基烷基、氨基烷基、烷氧基烷基、羧基或烷氧羰基，R6为羟基烷基、羧基、烷氧羰基或—( )q—NR7R8，其中q为1、2或3，且R7和R8各自独立地为H或烷基，或者R7和R8与它们所带的N原子形成一个环； - 当V为CR6时，U为 、NH或NR9，R0为H或烷氧基，R1为H或卤素，R2为H、烷基羰基或— —R3，R3为H或烷基羟基，R4为H或OH（当n不为0且R5为H时），R5为H、烷基、羟基烷基、氨基烷基、烷氧基烷基、羧基或烷氧羰基，R6为羟基烷基、羧基、烷氧羰基或—( )q—NR7R8，其中q为1、2或3，且R7和R8各自独立地为H或烷基，或者R7和R8与它们所带的N原子形成一个环； - 当V为一条键时，U为CH或N，R0为H或烷氧基，R1为H或卤素，R2为H、烷基羰基或— —R3，R3为H或烷基羟基，R4为H或OH（当n不为0且R5为H时），R5为H、烷基、羟基烷基、氨基烷基、烷氧基烷基、羧基或烷氧羰基，R6为羟基烷基、羧基、烷氧羰基或—( )q—NR7R8，其中q为1、2或3，且R7和R8各自独立地为H或烷基，或者R7和R8与它们所带的N原子形成一个环；A为—( )p—、— CH(OH)—或—CO CH(OH)—，G为取代苯基或G1或G2，其中Q为O或S，X为CH或N，Y1、Y2和Y3各自可以为CH或N；n当A为— CH(OH)—或—CO CH(OH)—时为0，当A为—( )p—时，n为0、1或2，p为1、2、3或4，但n和p的和必须为2、3或4；以及这些化合物的盐。