4(S)-4-Ethyl-4-hydroxy-7-[7-chloro-9-(4-methylpiperazin-1-ylmethyl)-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-ylmethyl]-4,7-dihydro-1H-pyrano[3,4-c]pyridine-3,8-dione | 195144-41-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 喹啉及其衍生物
• 英文名称: 4(S)-4-Ethyl-4-hydroxy-7-[7-chloro-9-(4-methylpiperazin-1-ylmethyl)-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-ylmethyl]-4,7-dihydro-1H-pyrano[3,4-c]pyridine-3,8-dione
• 英文别名: (4S)-7-[[7-chloro-9-[(4-methylpiperazin-1-yl)methyl]-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-yl]methyl]-4-ethyl-4-hydroxy-1H-pyrano[3,4-c]pyridine-3,8-dione
• CAS: 195144-41-3
• 化学式: C₂₈H₃₁ClN₄O₆
• 分子量: 555.03
• InChiKey: NCOIIQXEAPDJKQ-NDEPHWFRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.6
• 重原子数：
  39
• 可旋转键数：
  5
• 环数：
  6.0
• sp3杂化的碳原子比例：
  0.46
• 拓扑面积：
  105
• 氢给体数：
  1
• 氢受体数：
  9

反应信息

• 作为反应物：
  描述：

  4(S)-4-Ethyl-4-hydroxy-7-[7-chloro-9-(4-methylpiperazin-1-ylmethyl)-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-ylmethyl]-4,7-dihydro-1H-pyrano[3,4-c]pyridine-3,8-dione 在 palladium diacetate 、 potassium carbonate 、 三苯基膦 作用下， 以 乙腈 为溶剂， 反应 19.0h， 以55%的产率得到勒托替康
  参考文献：
  名称：

  Convergent catalytic asymmetric synthesis of camptothecin analog GI147211C

  摘要：

  The topoisomerase I inhibitor G1147211C (4) was discovered at Glare Wellcome and shown to have promising anti-cancer properties. In order to fully assess the clinical potential of 3, an improved synthesis of the: drug substance was required. Herein is described a convergent catalytic asymmetric synthesis of 4 which utilizes as key steps, two Heck reactions, a Sharpless asymmetric dihydroxylation reaction, and a Mitsunobu reaction. A 2-chloroquinoline is shown to be a viable substrate for the final Heck reaction to generate the camptothecin nucleus. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00357-8
• 作为产物：
  描述：

  7-chloro-9-chloromethyl-2,3-dihydro[1,4]dioxino[2,3-g]quinoline-8-carboxylic acid methyl ester 在 二异丁基氢化铝 、 三苯基膦 、 偶氮二甲酸二乙酯 作用下， 以 二氯甲烷 为溶剂， 反应 20.0h， 生成 4(S)-4-Ethyl-4-hydroxy-7-[7-chloro-9-(4-methylpiperazin-1-ylmethyl)-2,3-dihydro-[1,4]dioxino[2,3-g]quinolin-8-ylmethyl]-4,7-dihydro-1H-pyrano[3,4-c]pyridine-3,8-dione
  参考文献：
  名称：

  Convergent catalytic asymmetric synthesis of camptothecin analog GI147211C

  摘要：

  The topoisomerase I inhibitor G1147211C (4) was discovered at Glare Wellcome and shown to have promising anti-cancer properties. In order to fully assess the clinical potential of 3, an improved synthesis of the: drug substance was required. Herein is described a convergent catalytic asymmetric synthesis of 4 which utilizes as key steps, two Heck reactions, a Sharpless asymmetric dihydroxylation reaction, and a Mitsunobu reaction. A 2-chloroquinoline is shown to be a viable substrate for the final Heck reaction to generate the camptothecin nucleus. (C) 1997 Elsevier Science Ltd.

  DOI：

  10.1016/s0040-4020(97)00357-8

文献信息

• [EN] PREPARATION OF A CAMPTOTHECIN DERIVATIVE BY INTRAMOLECULAR CYCLISATION<br/>[FR] PREPARATION DE DERIVES DE LA CAMPTOTHECINE PAR CYCLISATION INTRAMOLECULAIRE
  申请人：GLAXO WELLCOME INC.

  公开号：WO1995029919A1

  公开（公告）日：1995-11-09

  (EN) The present invention relates to a method for the preparation of camptothecin and camptothecin-like compounds and to novel intermediates used in this preparation. In particular, the invention provides a process for the preparation of the camptothecin derivative of formula (I') known by the chemical name '7-(4-methylpiperazino-methylene)-10,11-ethylenedioxy-20(R,S)-camptothecin', which comprises cyclising the compound of formula (II'), wherein X is halogen, particularly chloro, bromo, or iodo; and when the compound of formula (I') is obtained as a mixture of enantiomers optionally resolving the mixture to obtain the desired enantiomer; and/or if desired, converting the resulting compound of formula (I') or a salt thereof into a physiologically acceptable salt or solvate thereof.(FR) L'invention porte sur une méthode de préparation de la camptothécine et de ses analogues, et sur de nouveaux intermédiaires servant à cette préparation; elle porte en particulier sur une méthode de préparation d'un dérivé de la camptothécine de formule (I') dit '7-(4-méthylpipérazinométhylène)-10,11-éthylénodioxy-20(R, S)-campothécine', obtenu par cyclisisation du composé de formule (II'), où X est halogène (en particulier chloro, bromo ou iodo), et dans lequel le composé de formule (I') est obtenu à partir d'un mélange d'énantiomères en résolvant éventuellement le mélange pour obtenir l'énantiomère désiré, et/ou en convertissant facultativement le composé résultant de formule (I') ou l'un de ses sels, en un sel physiologiquement acceptable ou en l'un de ses solvates.

  本发明涉及一种制备喜树碱和类喜树碱化合物的方法以及在该制备中使用的新型中间体。具体而言，本发明提供了一种制备喜树碱衍生物的方法，该衍生物的化学名称为“7-(4-甲基哌嗪亚甲基)-10,11-乙二氧基-20(R,S)-喜树碱”，其中包括将式(I')的化合物环化，其中X为卤素，特别是氯、溴或碘；如果式(I')的化合物以对映体混合物的形式获得，则可以选择性地分离混合物以获得所需的对映体；如果需要，则将所得的式(I')化合物或其盐转化为其生理上可接受的盐或溶剂化物。
• Preparation of a camptothecin derivative by intramolecular cyclisation
  申请人：OSI Pharmaceuticals, Inc.

  公开号：US20030045719A1

  公开（公告）日：2003-03-06

  The present invention relates to a method for the preparation for camptothecin and camptothecin-like compounds and to novel intermediates used in this preparation. In particular, the invention provides a process for the preparation of the camptothecin derivative of formula (I′) known by the chemical name “7-(4-methylpiperazinomethylene)-10,11-ethylenedioxy-20(R,S)-camptothecin”, which comprises cyclising the compound of formula (II′), wherein X is halogen, particularly chloro, bromo, or iodo; and when the compound of formula (I′) is obtained as a mixture of enantiomers optionally resolving the mixture to obtain the desired enantiomer; and/or if desired, converting the resulting compound of formula (I′) or a salt thereof into a physiologically acceptable salt or solvate thereof.

  本发明涉及一种制备喜树碱和类喜树碱的方法，以及在该制备中使用的新型中间体。具体而言，本发明提供了一种制备式(I')喜树碱衍生物的方法，该衍生物以化学名称“7-(4-甲基哌嗪亚甲基)-10,11-乙二氧基-20(R,S)-喜树碱”为已知，该方法包括将式(II')化合物环化，其中X为卤素，特别是氯、溴或碘；当式(I')化合物作为对映体混合物获得时，可以选择分离混合物以获得所需的对映体；以及/或者如果需要，将所得的式(I')化合物或其盐转化为其生理上可接受的盐或溶剂。
• PREPARATION OF A CAMPTOTHECIN DERIVATIVE BY INTRAMOLECULAR CYCLISATION
  申请人：GLAXO WELLCOME INC.

  公开号：EP0758335A1

  公开（公告）日：1997-02-19
• US6063923A
  申请人：——

  公开号：US6063923A

  公开（公告）日：2000-05-16
• US6462196B1
  申请人：——

  公开号：US6462196B1

  公开（公告）日：2002-10-08