11-aminomethyl-8-chloro-10,11-dihydro-dibenzo[b,f]oxepine-10-carboxylic acid methyl ester | 912356-04-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并吡喃
• 英文名称: 11-aminomethyl-8-chloro-10,11-dihydro-dibenzo[b,f]oxepine-10-carboxylic acid methyl ester
• 英文别名: methyl 10-aminomethyl-2-chloro-10,11-dihydrodibenzo[b,f]oxepine-11-carboxylate；methyl 6-(aminomethyl)-3-chloro-5,6-dihydrobenzo[b][1]benzoxepine-5-carboxylate
• CAS: 912356-04-8
• 化学式: C₁₇H₁₆ClNO₃
• 分子量: 317.772
• InChiKey: QWSQABREXKWIDM-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  22
• 可旋转键数：
  3
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.24
• 拓扑面积：
  61.6
• 氢给体数：
  1
• 氢受体数：
  4

反应信息

• 作为产物：
  描述：

  methyl 8-chloro-11-(nitromethyl)-10,11-dihydrodibenzo[b,f]oxepin-10-carboxylate 、 氢气 在 镍 四氢呋喃 作用下， 以 四氢呋喃 为溶剂， 反应 48.0h， 以to obtain methyl 10-aminomethyl-2-chloro-10,11-dihydrodibenzo[b,f]oxepine-11-carboxylate (compound XIIa), which的产率得到11-aminomethyl-8-chloro-10,11-dihydro-dibenzo[b,f]oxepine-10-carboxylic acid methyl ester
  参考文献：
  名称：

  PROCESSES FOR THE PREPARATION OF 5-CHLORO-2-METHYL-2,3,3A,12b-TETRAHYDRO-1H-DIBENZO[2,3:6,7]OXEPINO[4,5-c]PYRROLE

  摘要：

  本发明提供了改进的制备5-氯-2-甲基-2,3,3a,12b-四氢-1H-二苯并[2,3:6,7]氧杂[4,5-c]吡咯，即阿塞那平的工艺。这些工艺可以在工业规模下高产率和高立体选择性地制备阿塞那平。

  公开号：

  US20120165545A1

文献信息

• Intermediate compounds for the preparation of trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino[4,5-c]pyrrole
  申请人：Kemperman Johannes Gerardus

  公开号：US20060229352A1

  公开（公告）日：2006-10-12

  Disclosed are novel amino acid derivatives of formula (I) and (II) processes for the preparation thereof, and their use in the preparation of trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino-[4,5-c]pyrrole.

  本发明揭示了公式(I)和(II)的新型氨基酸衍生物，其制备方法，以及它们在制备trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino-[4,5-c]pyrrole中的应用。
• INTERMEDIATE COMPOUNDS FOR THE PREPARATION OF TRANS-5-CHLORO-2-METHYL-2,3,3a,12b-TETRAHYDRO-1H-DIBENZ[2,3:6,7]-OXEPINO[4,5-c]PYRROLE
  申请人：Kemperman Gerardus Johannes

  公开号：US20110207942A1

  公开（公告）日：2011-08-25

  Disclosed are novel amino acid derivatives of formula (I) and (II) processes for the preparation thereof, and their use in the preparation of trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino-[4,5-c]pyrrole.

  本发明涉及一种新型的氨基酸衍生物，其化学式为(I)和(II)，以及其制备方法，以及它们在制备trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino-[4,5-c]pyrrole中的用途。
• PROCESS FOR PRODUCING TRANS-DIBENZOXENOPYRROLE COMPOUND AND INTERMEDIATE THEREFOR
  申请人：Wang Weiqi

  公开号：US20110046393A1

  公开（公告）日：2011-02-24

  The invention provides a process for production of trans-dibenzoxenopyrrole compounds, in which reduction, leaving group conversion, hydrogenation and methylation are carried out in that order. The process of the invention allows trans-dibenzoxenopyrrole compounds to be produced by a simpler procedure than conventional processes. The invention further provides novel compounds obtained as intermediates in the process, and a process for their production.

  本发明提供了一种生产反式二苯并噁唑吡咯化合物的方法，其中按照还原、离去基转化、氢化和甲基化的顺序进行。本发明的方法比传统方法更简单，可以生产出反式二苯并噁唑吡咯化合物。本发明还提供了在该过程中获得的新型中间体化合物以及其生产方法。
• INTERMEDIATE COMPOUNDS FOR THE PREPARATION OF TRANS-5-CHLORO-2-METHYL-2,3,3A,12B-TETRAHYDRO-1H-DIBENZ[2,3:6,7]-OXEPINO[4,5-C]PYRROLE
  申请人：KEMPERMAN GERARDUS JOHANNES

  公开号：US20100152461A1

  公开（公告）日：2010-06-17

  Disclosed are novel amino acid derivatives of formula (I) and (II) processes for the preparation thereof, and their use in the preparation of trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino-[4,5-c]pyrrole.

  本发明涉及式(I)和(II)的新型氨基酸衍生物，其制备方法以及它们在制备trans-5-chloro-2-methyl-2,3,3a,12b-tetrahydro-1H-dibenz[2,3:6,7]oxepino-[4,5-c]pyrrole中的应用。
• Processes for the preparation of 5-chloro-2-methyl-2,3,3A,12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole
  申请人：Bosch i Lladó Jordi

  公开号：US08580972B2

  公开（公告）日：2013-11-12

  This invention provides improved processes for the preparation of 5-chloro-2-methyl-2,3,3a 12b-tetrahydro-1H-dibenzo[2,3:6,7]oxepino[4,5-c]pyrrole, asenapine. These processes allow the preparation of asenapine at industrial scale in good yields and high stereoselectivity.

  本发明提供了改进的工艺，用于制备5-氯-2-甲基-2,3,3a 12b-四氢-1H-二苯并[2,3:6,7]氧杂[4,5-c]吡咯，即阿塞那平。这些工艺允许在工业规模下以良好的产率和高立体选择性制备阿塞那平。