((3R,4S)-4-Trifluoromethyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester | 168544-95-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 吡咯烷类
• 英文名称: ((3R,4S)-4-Trifluoromethyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester
• 英文别名: tert-butyl N-[trans-4-(trifluoromethyl)pyrrolidin-3-yl]carbamate；tert-butyl N-[(3R,4S)-4-(trifluoromethyl)pyrrolidin-3-yl]carbamate
• CAS: 168544-95-4
• 化学式: C₁₀H₁₇F₃N₂O₂
• 分子量: 254.252
• InChiKey: TTZLWOFPFKRYBC-BQBZGAKWSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.7
• 重原子数：
  17
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.9
• 拓扑面积：
  50.4
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  ((3R,4S)-4-Trifluoromethyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester 在 三乙胺 作用下， 以 二甲基亚砜 为溶剂， 生成 7-((3R,4S)-3-Amino-4-trifluoromethyl-pyrrolidin-1-yl)-1-cyclopropyl-6-fluoro-8-methoxy-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid; compound with trifluoro-acetic acid
  参考文献：
  名称：

  Synthesis and antibacterial activity of novel 7-(3-substituted-3 or 4-trifluoromethyl-1-pyrrolidinyl)-8-methoxyfluoroquinolones

  摘要：

  The titled compounds were synthesized and evaluated for in vitro antibacterial activity. The (3R,4S)-3-aminomethyl-4-trifluoromethyl derivative (S-34109) was confirmed to be optimal because of its superior activity against quinolone and methicillin-resistant Staphyrococcus aureus and low side effect potential. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00514-9
• 作为产物：
  描述：

  (3S,4S)-1-Benzyl-4-trifluoromethyl-pyrrolidine-3-carboxylic acid 在 palladium on activated charcoal 二苯基磷酸 、 氢气 、 三乙胺 作用下， 以 甲醇 为溶剂， 生成 ((3R,4S)-4-Trifluoromethyl-pyrrolidin-3-yl)-carbamic acid tert-butyl ester
  参考文献：
  名称：

  Synthesis and antibacterial activity of novel 7-(3-substituted-3 or 4-trifluoromethyl-1-pyrrolidinyl)-8-methoxyfluoroquinolones

  摘要：

  The titled compounds were synthesized and evaluated for in vitro antibacterial activity. The (3R,4S)-3-aminomethyl-4-trifluoromethyl derivative (S-34109) was confirmed to be optimal because of its superior activity against quinolone and methicillin-resistant Staphyrococcus aureus and low side effect potential. (C) 1998 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(98)00514-9

文献信息

• [EN] QUINOLIZINONE TYPE COMPOUNDS<br/>[FR] COMPOSES DU TYPE DE LA QUINOLIZINONE
  申请人：ABBOTT LABORATORIES

  公开号：WO1995010519A1

  公开（公告）日：1995-04-20

  (EN) Antibacterical coumpounds having formula (I) and the pharmaceutically acceptable salts, esters and amides thereof, preferred examples of which include those coumpounds wherein R1 is cycloalkyl of from three to eight carbon atoms or substituted phenyl; R2is selected from the group consisting of (a) halogen, (b) loweralkyl, (c) loweralkenyl, (d) cycloalkyl of from three to eight carbons, (e) cycloalkenyl of from four to eight carbons, (f) loweralkoxy, (g) aryloxy, (h) aryl(loweralkyl)oxy, (i) aryl(loweralkyl), (j) cycloalkyl(loweralkyl), (k) amino, (l) (loweralkyl)amino, (m) aryl(loweralkyl)amino, (n) hydroxy substituted (loweralkyl)amino, (o) phenyl, (p) substituted phenyl, (q) bicyclic nitrogen-containing heterocycle, (r) nitrogen-containingaromatic heterocycle, and (s) nitrogen-containing heterocycle having formula (Ia) where x is between zero and three; R3 is halogen; R4 is hydrogen, loweralkyl, a pharmaceutically acceptable cation, or a prodrug ester group; R5 is hydrogen, loweralkyl, halo(loweralkyl), or -NR13R14; and R6 is loweralkyl, as wellas pharmaceutical compositions containing such compounds and the use of the same in the treatment of bacterial infections.(FR) Composés antibactériens de la formule (I) et sels, esters et amides pharmaceutiquement acceptables de ceux-ci, dont des exemples préférés comprennent des composés dans lesquels: R1 est un cycloalcoyle avec deux à huit atomes de carbone ou un phényle substitué; R2 est sélectionné dans le groupe comprenant: (a) halogène, (b) alcoyle inférieur, (c) alcényle inférieur, (c) cycloalcoyle avec trois à huit atomes de carbone, (e) cycloalcényle avec quatre à huit atomes de carbone, (f) alcoxy inférieur, (g) aroyloxy, (h) aroyl(alcoyle inférieur)oxy, (I) aroyl(alcoyle inférieur), (j) cycloalcoyle(alcoyle inférieur), (k) amino, (l) (alcoyle inférieur)amino, (m) aroyl(alcoyle inférieur)amino, (n) (alcoyle inférieur)amino substitué par hydroxy, (o) phényle, (p) phényle substitué, (q) hétérocycle dicyclique azoté, (r) hétérocycle aromatique azoté et (s) hétérocycle azoté de la formule (Ia), dans laquelle R3 est un halogène; R4 est l'hydrogène, un alcoyle inférieur, un cation pharmaceutiquement acceptable ou un groupe ester promédicamenteux; R5 est l'hydrogène, un alcoyle inférieur, un halo(alcoyle inférieur) ou -NR13R14; et R6 est un alcoyle inférieur. L'invention décrit également des compositions pharmaceutiques contenant ces composés et l'utilisation de celles-ci dans le traitement des infections bactériennes.

  (中) 具有公式(I)及其药学上可接受的盐、酯和酰胺的抗菌化合物，其中R1是由三到八个碳原子的环烷基或取代的苯基; R2选自以下组中：(a)卤素，(b)较低的烷基，(c)较低的烯基，(d)由三到八个碳原子的环烷基，(e)由四到八个碳原子的环烯基，(f)较低的烷氧基，(g)芳氧基，(h)芳基(较低的烷氧基)，(i)芳基(较低的烷基)，(j)环烷基(较低的烷基)，(k)氨基，(l)(较低的烷基)氨基，(m)芳基(较低的烷基)氨基，(n)羟基取代的(较低的烷基)氨基，(o)苯基，(p)取代的苯基，(q)含氮的双环杂环，(r)含氮芳香杂环，(s)具有公式(Ia)的含氮杂环，其中x在零到三之间; R3是卤素; R4是氢、较低的烷基、药学上可接受的阳离子或前药酯基; R5是氢、较低的烷基、卤代(较低的烷基)或-NR13R14; R6是较低的烷基，以及包含这种化合物的药物组合物和在治疗细菌感染中使用它们的用途。
• [EN] 3-AMINOQUINAZOLIN-2,4-DIONE ANTIBACTERIAL AGENTS<br/>[FR] AGENTS ANTIBACTERIENS CONTENANT 3-AMINOQUINAZOLIN-2,4-DIONE
  申请人：WARNER LAMBERT CO

  公开号：WO2001053273A1

  公开（公告）日：2001-07-26

  Antibacterial 3-aminoquinazolin-2,4-diones have formula (I) wherein: R1 and R3 include alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclic, and heteroaryl; R5, R6, and R8 include H, alkyl, alkoxy, halo, NO2, CN, NH2, alkyl and dialkylamino; R7 includes hydrogen, alkyl, cycloalkyl, heterocyclic, fused heterocyclic, aryl and fused aryl; J and K are C or N; and pharmaceutically acceptable salts thereof.

  具有式(I)的抗菌3-氨基喹唑啉-2,4-二酮，其中：R1和R3包括烷基，烯基，炔基，环烷基，芳基，杂环基和杂芳基；R5，R6和R8包括H，烷基，烷氧基，卤素，NO2，CN，NH2，烷基和二烷基氨基；R7包括氢，烷基，环烷基，杂环基，融合的杂环基，芳基和融合的芳基；J和K是C或N；以及其药学上可接受的盐。
• 3-AMINOQUINAZOLIN-2,4-DIONE ANTIBACTERIAL AGENTS
  申请人：Bird Paul

  公开号：US20060183762A1

  公开（公告）日：2006-08-17

  Antibacterial 3-aminoquinazolin-2,4-diones have formula (I) wherein: R 1 and R 3 include alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclic, and heteroaryl; R 5 , R 6 , and R 8 include H, alkyl, alkoxy, halo, NO 2 , CN, NH 2 , alkyl and dialkylamino; R 7 includes hydrogen, alkyl, cycloalkyl, heterocyclic, fused heterocyclic, aryl and fused aryl; J and K are C or N; and pharmaceutically acceptable salts thereof.

  抗菌3-氨基喹唑啉-2,4-二酮具有以下化学式（I）：其中：R1和R3包括烷基，烯基，炔基，环烷基，芳基，杂环基和杂芳基；R5，R6和R8包括H，烷基，烷氧基，卤素，NO2，CN，NH2，烷基和二烷基氨基；R7包括氢，烷基，环烷基，杂环基，融合的杂环基，芳基和融合的芳基；J和K为C或N；以及其药学上可接受的盐。
• 3-Aminoquinazolin-2,4-dione antibacterial agents
  申请人：Bird Paul

  公开号：US20060287308A1

  公开（公告）日：2006-12-21

  Antibacterial 3-aminoquinazolin-2,4-diones have formula (1) wherein: R 1 and R 3 include alkyl, alkenyl, alkynyl, cycloalkyl, aryl, heterocyclic, and heteroaryl; R 5 , R 6 , and R 8 include H, alkyl, alkoxy, halo, NO 2 , CN, NH 2 , alkyl and dialkylamino; R 7 includes hydrogen, alkyl, cycloalkyl, heterocyclic, fused heterocyclic, aryl and fused aryl; J and K are C or N; and pharmaceutically acceptable salts thereof.

  抗菌的3-氨基喹唑啉-2,4-二酮具有式（1），其中：R1和R3包括烷基，烯基，炔基，环烷基，芳香基，杂环基和杂芳基；R5，R6和R8包括H，烷基，烷氧基，卤素，NO2，CN，NH2，烷基和二烷基氨基；R7包括氢，烷基，环烷基，杂环基，融合杂环基，芳香基和融合芳香基；J和K是C或N；以及其药学上可接受的盐。
• QUINOLINECARBOXYLIC ACID DERIVATIVE AND SALT THEREOF
  申请人：KAKEN PHARMACEUTICAL CO., LTD.

  公开号：EP0726269A1

  公开（公告）日：1996-08-14

  Quinolinecarboxylic acid derivatives which are represented by the general formula (I) wherein R1 is a C1 to C6 alkyl group which may be substituted, a C2 to C6 alkenyl group which may be substituted, a C3 to C7 cycloalkyl group which may be substituted or an aryl group which may be substituted, R2 is hydrogen atom; a halogen atom; hydroxyl group which may be protected, amino group or a C1 to C6 alkylamino group each of which may be protected; a C1 to C6 dialkylamino group or a C1 to C6 alkyl group, R3 is hydrogen atom or a C1 to C6 alkyl group, A is nitrogen atom or wherein A' is hydrogen atom, a halogen atom, a C1 to C6 alkyl group, a C1 to C6 alkoxyl group which may be substituted, cyano group, or nitro group, and A' may form a ring with R1; the ring may include oxygen atom, nitrogen atom, or sulfur atom as a constituent atom; the ring may be substituted with a C1 to C6 alkyl group, X is hydroxymethyl group; aminomethyl group or amino group each of which may be protected, and salts thereof, and antibacterial agents which comprise the quinolinecarboxylic acid derivatives and salts thereof as active ingredients, and therapeutical methods thereby.

  通式(I)表示的喹啉羧酸衍生物 其中 R1 是可被取代的 C1 至 C6 烷基、可被取代的 C2 至 C6 烯基、可被取代的 C3 至 C7 环烷基或可被取代的芳基，R2 是氢原子；卤素原子；可被保护的羟基、氨基或 C1 至 C6 烷基氨基，其中每个都可被保护；C1 至 C6 二烷基氨基或 C1 至 C6 烷基、 R3 是氢原子或 C1 至 C6 烷基、 A 是氮原子或 其中 A'是氢原子、卤素原子、C1 至 C6 烷基、可被取代的 C1 至 C6 烷氧基、氰基或硝基，A'可与 R1 形成环；环的组成原子可包括氧原子、氮原子或硫原子；环可被 C1 至 C6 烷基取代、 X 是羟甲基、氨甲基或氨基，其中每个基团都可以被保护、 及其盐类，以及包含喹啉羧酸衍生物及其盐类作为活性成分的抗菌剂及其治疗方法。