((1S,3S,5S)-3-(三苯甲基)-6-氧杂二环[3.1.0]己烷-1-基)甲醇 | 1113025-23-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 三苯基化合物
• 中文名称: ((1S,3S,5S)-3-(三苯甲基)-6-氧杂二环[3.1.0]己烷-1-基)甲醇
• 英文名称: [(1S,3S,5S)-3-(tritylamino)-6-oxabicyclo[3.1.0]hex-1-yl]methanol
• 英文别名: [(1S,3S,5S)-3-(Tritylamino)-6-oxabicyclo[3.1.0]hexan-1-yl]methanol；[(1S,3S,5S)-3-(tritylamino)-6-oxabicyclo[3.1.0]hexan-1-yl]methanol
• CAS: 1113025-23-2
• 化学式: C₂₅H₂₅NO₂
• 分子量: 371.479
• InChiKey: HIDDPUDMYMCTNU-HJOGWXRNSA-N

物化性质

• 沸点：
  522.7±50.0 °C(Predicted)
• 密度：
  1.24±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.9
• 重原子数：
  28
• 可旋转键数：
  6
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.28
• 拓扑面积：
  44.8
• 氢给体数：
  2
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  ((1S,3S,5S)-3-(三苯甲基)-6-氧杂二环[3.1.0]己烷-1-基)甲醇 在 硼烷四氢呋喃络合物 、 palladium on activated charcoal 、 氢气 、 三乙胺 作用下， 以 甲醇 、 二氯甲烷 、 异丙醇 为溶剂， 生成 (1S,2S,4R)-4-(4-chloro-7H-pyrrolo[2,3-d]pyrimidin-7-yl)-2-(hydroxymethyl)cyclopentanol
  参考文献：
  名称：

  Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat

  摘要：

  A practical synthesis of a novel NEDD8-activating enzyme (NAE) inhibitor pevonedistat (MLN4924) is described. Key steps include an enantioselective synthesis of an amino-diol cyclopentane intermediate containing three chiral centers and a novel, regioselective sulfamoylation using N-(tert-butoxycarbonyl)-N-[(triethylenediammonium)sulfonyl]azanide. The linear process, involving six solid isolations, has been carried out in multiple cGMP productions on 15-30 kg scale to produce pevonedistat in 98% (a/a) chemical purity and 25% overall yield.

  DOI：

  10.1021/acs.oprd.5b00209
• 作为产物：
  描述：

  (1S,4R)-4-甲基环戊-2-烯甲酸甲酯盐酸盐 在 叔丁基过氧化氢 、 L-(+)-酒石酸二乙酯 、 二异丁基氢化铝 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 二氯甲烷 、 甲苯 为溶剂， 生成 ((1S,3S,5S)-3-(三苯甲基)-6-氧杂二环[3.1.0]己烷-1-基)甲醇
  参考文献：
  名称：

  Process Development and GMP Production of a Potent NAE Inhibitor Pevonedistat

  摘要：

  A practical synthesis of a novel NEDD8-activating enzyme (NAE) inhibitor pevonedistat (MLN4924) is described. Key steps include an enantioselective synthesis of an amino-diol cyclopentane intermediate containing three chiral centers and a novel, regioselective sulfamoylation using N-(tert-butoxycarbonyl)-N-[(triethylenediammonium)sulfonyl]azanide. The linear process, involving six solid isolations, has been carried out in multiple cGMP productions on 15-30 kg scale to produce pevonedistat in 98% (a/a) chemical purity and 25% overall yield.

  DOI：

  10.1021/acs.oprd.5b00209

文献信息

• Process for the synthesis of E1 activating enzyme inhibitors
  申请人：Armitage Ian

  公开号：US20090036678A1

  公开（公告）日：2009-02-05

  The present invention provides processes and synthetic intermediates for the synthesis of 4-substituted ((1S,2S,4R)-2-hydroxy-4-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl)methyl sulfamates, which are E1 activating enzyme inhibitors, and are useful for the treatment of disorders of cell proliferation, particularly cancer, and other disorders associated with E1 activity.

  本发明提供了用于合成4-取代((1S,2S,4R)-2-羟基-4-7H-吡咯并[2,3-d]嘧啶-7-基}环戊基)甲基磺酸酯的过程和合成中间体，该化合物是E1激活酶抑制剂，可用于治疗细胞增殖紊乱，特别是癌症，以及与E1活性相关的其他紊乱。
• PROCESS FOR THE SYNTHESIS OF E1 ACTIVATING ENZYME INHIBITORS
  申请人：Millennium Pharmaceuticals, Inc.

  公开号：US20180079755A1

  公开（公告）日：2018-03-22

  The present invention provides processes and synthetic intermediates for the synthesis of 4-substituted ((4S, 2S, 4R)-2-hydroxy-4-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl)methyl sulfamates, which are E1 activating enzyme inhibitors, and are useful for the treatment of disorders of cell proliferation, particularly cancer, and other disorders associated with E1 activity.

  本发明提供了合成4-取代基((4S, 2S, 4R)-2-羟基-4-7H-吡咯并[2,3-d]嘧啶-7-基}环戊基)甲基磺酸酯的过程和合成中间体，这些化合物是E1激活酶抑制剂，可用于治疗细胞增殖失调疾病，特别是癌症和与E1活性相关的其他疾病。
• Process for the synthesis of intermediates compounds useful for the preparation of E1 activity activating enzyme inhibitors
  申请人：MILLENNIUM PHARMACEUTICALS, INC.

  公开号：EP2546256A2

  公开（公告）日：2013-01-16

  The present invention provides processes and synthetic intermediates for the synthesis of 4-substituted ((1S, 2S, 4R)-2-hydroxy-4-7H-pyrrolo[2,3-d]pyrimidin-7-yl}cyclopentyl)methyl sulfamates, which are E1 activating enzyme inhibitors, and are useful for the treatment of disorders of cell proliferation, particularly cancer, and other disorders associated with E1 activity.

  本发明提供了合成 4-取代((1S, 2S, 4R)-2-羟基-4-7H-吡咯并[2,3-d]嘧啶-7-基}环戊基)甲基氨基磺酸盐的工艺和合成中间体，它们是 E1 活化酶抑制剂，可用于治疗细胞增殖紊乱，特别是癌症，以及其他与 E1 活性相关的疾病。
• Intermediates for the synthesis of E1 activity activating enzyme inhibitors
  申请人：MILLENNIUM PHARMACEUTICALS, INC.

  公开号：EP2540726B1

  公开（公告）日：2019-10-09
• SULFAMOYLATING REAGENT
  申请人：MILLENNIUM PHARMACEUTICALS, INC.

  公开号：EP2540727B1

  公开（公告）日：2018-07-25