7-cyclopentyl-2-(1',2',3',4',5',6'-hexahydro-[3,4']bipyridinyl-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide | 1211441-43-8

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二嗪类
• 英文名称: 7-cyclopentyl-2-(1',2',3',4',5',6'-hexahydro-[3,4']bipyridinyl-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide
• 英文别名: 7-cyclopentyl-N,N-dimethyl-2-[(5-piperidin-4-ylpyridin-2-yl)amino]pyrrolo[2,3-d]pyrimidine-6-carboxamide
• CAS: 1211441-43-8
• 化学式: C₂₄H₃₁N₇O
• 分子量: 433.556
• InChiKey: YKWPDJQXUDYJND-UHFFFAOYSA-N

物化性质

• 沸点：
  691.7±65.0 °C(Predicted)
• 密度：
  1.36±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  32
• 可旋转键数：
  5
• 环数：
  5.0
• sp3杂化的碳原子比例：
  0.5
• 拓扑面积：
  88
• 氢给体数：
  2
• 氢受体数：
  6

反应信息

• 作为反应物：
  描述：

  7-cyclopentyl-2-(1',2',3',4',5',6'-hexahydro-[3,4']bipyridinyl-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide 、 丙酮 在 溶剂黄146 三乙酰氧基硼氢化钠 、 sodium hydroxide 作用下， 以 二氯甲烷 、 水 为溶剂， 以70%的产率得到7-cyclopentyl-2-[6-(4-isopropylpiperazin-1-yl)pyridazin-3-ylamino]-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide
  参考文献：
  名称：

  [EN] PYRROLOPYRIMIDINE COMPOUNDS AS CDK INHIBITORS
  [FR] COMPOSÉS DE PYRROLOPYRIMIDINE ET LEURS UTILISATIONS

  摘要：

  所披露的化合物涉及治疗与蛋白激酶相关的疾病。此外，还需要用于治疗、预防或改善癌症、移植排斥和自身免疫疾病的一个或多个症状的化合物。更进一步，还需要使用本处提供的化合物来调节蛋白激酶活性的方法，如CDK1、CDK2、CDK4、CDK5、CDK6、CDK7、CDK8和CDK9。

  公开号：

  WO2010020675A1
• 作为产物：
  描述：

  2-氯-7-环戊基-N,N-二甲基-7H-吡咯并[2,3-d]嘧啶-6-甲酰胺 、 4-(6-氨基吡啶-3-基)哌啶-1-羧酸叔丁酯 以to give 7-cyclopentyl-2-(1′,2′,3′,4′,5′,6′-hexahydro-[3,4′]bipyridinyl-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide (212 mg, 48%)的产率得到7-cyclopentyl-2-(1',2',3',4',5',6'-hexahydro-[3,4']bipyridinyl-6-ylamino)-7H-pyrrolo[2,3-d]pyrimidine-6-carboxylic acid dimethylamide
  参考文献：
  名称：

  Pyrrolopyrimidine compounds and their uses

  摘要：

  本发明涉及公式(I)的化合物，以及其药学上可接受的盐和制药组合物。本发明还涉及使用公式(I)的化合物来调节蛋白激酶的活性，并用于治疗疾病，特别是与CDK4抑制相关的疾病、障碍或综合征的治疗。

  公开号：

  US08415355B2

文献信息

• PYRROLOPYRIMIDINE COMPOUNDS AND THEIR USES
  申请人：NOVARTIS AG

  公开号：US20130184285A1

  公开（公告）日：2013-07-18

  The disclosed compounds relate to treatments and therapies for protein kinase-associated disorders. There is also a need for compounds useful in the treatment or prevention or amelioration of one or more symptoms of cancer, transplant rejections, and autoimmune diseases. Furthermore, there is a need for methods for modulating the activity of protein kinases, such as CDK1, CDK2, CDK4, CDK5, CDK6, CDK7, CDK8 and CDK9, using the compounds provided herein.

  所透露的化合物涉及蛋白激酶相关疾病的治疗和疗法。还需要用于治疗、预防或改善癌症、移植排斥和自身免疫性疾病一种或多种症状的化合物。此外，还需要使用此处提供的化合物调节蛋白激酶活性的方法，如CDK1、CDK2、CDK4、CDK5、CDK6、CDK7、CDK8和CDK9。
• Preservation of immune response during chemotherapy regimens
  申请人：G1 Therapeutics, Inc.

  公开号：US11529352B2

  公开（公告）日：2022-12-20

  The addition of a selective, fast-acting, short half-life CDK 4/6 inhibitor in a very specific dosage regimen to the combination of chemotherapy with a checkpoint inhibitor provides superior results in the treatment of a tumor or cancer. The unexpected discovery is that the short pulsatile specifically-timed administration of a selective, fast-acting, short half-life CDK 4/6 inhibitor during administration of the chemotherapy portion of the triple combination therapy has a profound effect on the immune cells in the cancer microenvironment.

  在化疗与检查点抑制剂的联合治疗中加入选择性、起效快、半衰期短的CDK 4/6抑制剂，并采用非常特异的剂量方案，可为肿瘤或癌症的治疗提供卓越的效果。意想不到的发现是，在三联疗法中化疗部分的给药过程中，选择性、速效、短半衰期 CDK 4/6 抑制剂的短脉冲特异定时给药对癌症微环境中的免疫细胞有深远影响。
• PYRROLOPYRIMIDINE COMPOUNDS AS CDK INHIBITORS
  申请人：Novartis AG

  公开号：EP2331547B1

  公开（公告）日：2014-07-30
• PRESERVATION OF IMMUNE RESPONSE DURING CHEMOTHERAPY REGIMENS
  申请人：G1 Therapeutics, Inc.

  公开号：US20190321370A1

  公开（公告）日：2019-10-24

  The addition of a selective, fast-acting, short half-life CDK 4/6 inhibitor in a very specific dosage regimen to the combination of chemotherapy with a checkpoint inhibitor provides superior results in the treatment of a tumor or cancer. The unexpected discovery is that the short pulsatile specifically-timed administration of a selective, fast-acting, short half-life CDK 4/6 inhibitor during administration of the chemotherapy portion of the triple combination therapy has a profound effect on the immune cells in the cancer microenvironment.
• PHARMACEUTICAL COMBINATION COMPRISING LSZ102 AND RIBOCICLIB
  申请人：NOVARTIS AG

  公开号：US20220031657A1

  公开（公告）日：2022-02-03

  The present invention relates to a pharmaceutical combination comprising LSZ102 and ribociclib; pharmaceutical compositions comprising the same; and methods of using such combinations and compositions in the treatment or prevention of conditions in which degradation of estrogen receptors combined with CDK4/6 inhibition is beneficial in, for example, the treatment of cancers.