3-氟-4-(吗啉-4-羰基)苯基硼酸 | 1008119-70-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 3-氟-4-(吗啉-4-羰基)苯基硼酸
• 英文名称: (3-fluoro-4-(morpholine-4-carbonyl)phenyl)boronic acid
• 英文别名: 3-fluoro-4-(morpholine-4-carbonyl)phenylboronic acid；[3-fluoro-4-(morpholine-4-carbonyl)phenyl]boronic acid
• CAS: 1008119-70-7
• 化学式: C₁₁H₁₃BFNO₄
• 分子量: 253.038
• InChiKey: PCOQCLUJTVPMSY-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  -1.02
• 重原子数：
  18
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  70
• 氢给体数：
  2
• 氢受体数：
  5

安全信息

• 海关编码：
  2934999090
• 危险性防范说明：
  P261,P264,P270,P271,P280,P301+P312,P302+P352,P304+P340,P305+P351+P338,P330,P332+P313,P337+P313,P362,P403+P233,P405,P501
• 危险性描述：
  H302,H315,H319,H335
• 储存条件：
  2-8°C

SDS

3-氟-4-(吗啉-4-羰基)苯基硼酸MSDS英文版

反应信息

• 作为反应物：
  描述：

  3-氟-4-(吗啉-4-羰基)苯基硼酸 在 potassium phosphate 、 四(三苯基膦)钯 、 N,N-二异丙基乙胺 、 N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate 作用下， 以 N,N-二甲基甲酰胺 、 乙腈 为溶剂， 反应 32.0h， 生成 (S)-5-(2-(2-(3-fluoro-4-(morpholine-4-carbonyl)phenyl)-5H-chromeno[2,3-b]pyridin-5-yl)-2-methylpropanamido)-N-methyl-1,3,4-thiadiazole-2-carboxamide
  参考文献：
  名称：

  Improving the Pharmacokinetic and CYP Inhibition Profiles of Azaxanthene-Based Glucocorticoid Receptor Modulators—Identification of (S)-5-(2-(9-Fluoro-2-(4-(2-hydroxypropan-2-yl)phenyl)-5H-chromeno[2,3-b]pyridin-5-yl)-2-methylpropanamido)-N-(tetrahydro-2H-pyran-4-yl)-1,3,4-thiadiazole-2-carboxamide (BMS-341)

  摘要：

  An empirical approach to improve the microsomal stability and CYP inhibition profile of lead compounds 1a and 1b led to the identification of 5 (BMS-341) as a dissociated glucocorticoid receptor modulator. Compound 5 showed significant improvements in pharmacokinetic properties and, unlike compounds 1a-b, displayed a linear, dose-dependent pharmacokinetic profile in rats. When tested in a chronic model of adjuvant-induced arthritis in rat, the ED50 of 5 (0.9 mg/kg) was superior to that of both 1a and 1b (8 and 17 mg/kg, respectively).

  DOI：

  10.1021/acs.jmedchem.5b00257
• 作为产物：
  描述：

  吗啉 、 4-羧基-3-氟苯硼酸 在 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下， 以 N,N-二甲基甲酰胺 为溶剂， 反应 18.0h， 生成 3-氟-4-(吗啉-4-羰基)苯基硼酸
  参考文献：
  名称：

  [EN] AMINOPYRIDINE DERIVED COMPOUNDS AS LRRK2 INHIBITORS
  [FR] COMPOSÉS DÉRIVÉS DE L'AMINOPYRIDINE UTILISÉS EN TANT QU'INHIBITEURS DE LRRK2

  摘要：

  本发明涉及公式（A）的氨基吡啶衍生物化合物。这些化合物被认为对与LRRK2相关的疾病如小体痴呆、帕金森病或癌症的治疗具有用处。

  公开号：

  WO2014106612A1

文献信息

• [EN] FUSED HETEROARYL MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-KB ACTIVITY AND USE THEREOF<br/>[FR] MODULATEURS HÉTÉROARYLE CONDENSÉS, DE L'ACTIVITÉ AP-1 ET/OU NF-?B DU RÉCEPTEUR DES GLUCOCORTICOÏDES ET LEUR UTILISATION
  申请人：BRISTOL MYERS SQUIBB CO

  公开号：WO2009100171A1

  公开（公告）日：2009-08-13

  Novel non-steroidal compounds are provided which are useful in treating diseases or disorders associated with modulation of the glucocorticoid receptor, AP-1, and/or NF-κB activity, including metabolic and inflammatory and immune diseases or disorders, having the structure of formula (I): an enantiomer, diastereomer, or taυtomer thereof, or a prodrug ester thereof, or a pharmaceutically-acceptable salt thereof, in which: Z is heterocyclo or heteroaryl; • A is a S- to 8- membered carbocyclic ring or a S- to 8-membered heterocyclic ring; B1 and B2 rings are pyridyl rings, wherein the B1 and B2 rings are each fused to the A ring and the B1 ring is optionally substituted by one to three groups which are the same or different and are independently selected from R1, R2, and R4, and the B2 ring is optionally substituted by one to three groups which are the same or different and are independently selected from R5, R7, and R3 J1, J2, and J3 are at each occurrence the same or different and are independently - A1QA2-; Q is a bond, O, S, S(O), or S(O)2; A1 and A2 are the same or different and are at each occurrence independently selected from a bond, C1-3 alkylene, substituted C1-3 alkylene, C2-4 alkenylene, and substituted C2-4 alkenylene, provided that A1 and A2 are chosen so that ring A is a 5- to 8-membered carbocyclic or heterocyclic ring; R1 to R11 are as defined herein....

  提供了一种新型的非类固醇化合物，可用于治疗与糖皮质激素受体、AP-1和/或NF-κB活性调节相关的疾病或紊乱，包括代谢性、炎症性和免疫性疾病或紊乱，其结构如下式（I）：其对映体、非对映体或互变异构体，或其前药酯，或其药用可接受盐，其中：Z是杂环或杂芳基；• A是S至8-成员碳环或S至8-成员杂环；B1和B2环是吡啶环，其中B1和B2环各与A环融合，B1环可选地由一个至三个基取代，所述基相同或不同，并且独立地从R1、R2和R4中选择，B2环可选地由一个至三个基取代，所述基相同或不同，并且独立地从R5、R7和R3中选择，J1、J2和J3在每次出现时相同或不同，并且独立地为-A1QA2-；Q是键，O，S，S（O）或S（O）2；A1和A2相同或不同，并且在每次出现时独立地从键，C1-3烷基，取代C1-3烷基，C2-4烯烃基和取代C2-4烯烃基中选择，前提是选择A1和A2以使环A为5-至8-成员碳环或杂环；R1至R11如此处所定义...
• Fused heteroaryl modulators of glucocorticoid receptor, AP-1, and/or NF-κB activity and use thereof
  申请人：Bristol-Myers Squibb Company

  公开号：US08304539B2

  公开（公告）日：2012-11-06

  Novel non-steroidal compounds are provided which are useful in treating diseases or disorders associated with modulation of the glucocorticoid receptor, AP-1, and/or NF-κB activity, including metabolic and inflammatory and immune diseases or disorders, having the structure of formula (I): an enantiomer, diastereomer, or taυtomer thereof, or a prodrug ester thereof, or a pharmaceutically-acceptable salt thereof, in which: Z is heterocyclo or heteroaryl; •A is a S- to 8-membered carbocyclic ring or a S- to 8-membered heterocyclic ring; B1 and B2 rings are pyridyl rings, wherein the B1 and B2 rings are each fused to the A ring and the B1 ring is optionally substituted by one to three groups which are the same or different and are independently selected from R1, R2, and R4, and the B2 ring is optionally substituted by one to three groups which are the same or different and are independently selected from R5, R7, and R3 J1, J2, and J3 are at each occurrence the same or different and are independently -A1QA2-; Q is a bond, O, S, S(O), or S(O)2; A1 and A2 are the same or different and are at each occurrence independently selected from a bond, C1-3 alkylene, substituted C1-3 alkylene, C2-4 alkenylene, and substituted C2-4 alkenylene, provided that A1 and A2 are chosen so that ring A is a 5- to 8-membered carbocyclic or heterocyclic ring; R1 to R11 are as defined herein.

  提供了新型非甾体化合物，其在治疗与糖皮质激素受体、AP-1和/或NF-κB活性调节相关的疾病或障碍中非常有用，包括代谢性、炎症性和免疫性疾病或障碍，其结构为公式（I）：其对映体、顺异构体或互变异构体，或其前药酯，或其药学上可接受的盐，其中：Z是杂环或杂芳基；•A是S-至8元环碳环或S-至8元杂环；B1和B2环是吡啶环，其中B1和B2环各与A环融合，B1环可选地被一到三个相同或不同的基团取代，这些基团独立地从R1、R2和R4中选择，B2环可选地被一到三个相同或不同的基团取代，这些基团独立地从R5、R7和R3 J1、J2和J3在每次出现时都相同或不同，并且独立地是-A1QA2-；Q是键，O，S，S（O）或S（O）2；A1和A2在每次出现时相同或不同，并且独立地从键，C1-3烷基，取代C1-3烷基，C2-4烯基和取代C2-4烯基中选择，前提是A1和A2被选择为环A是5-至8元环碳环或杂环；R1至R11如本文所定义。
• Aminopyridine Derived Compounds as LRRK2 Inhibitors
  申请人：H. Lundbeck A/S

  公开号：US20160184317A1

  公开（公告）日：2016-06-30

  The present invention is directed to aminopyridine derived compounds of formula (A) The compounds are considered useful for the treatment of diseases associated with LRRK2 such a Lewy body dementia, Parkinson's disease or cancer.

  本发明涉及公式（A）的氨基吡啶衍生物化合物。这些化合物被认为对于与LRRK2相关的疾病的治疗是有用的，例如Lewy体痴呆症、帕金森病或癌症。
• Aminopyridine derived compounds as LRRK2 inhibitors
  申请人：H. Lundbeck A/S

  公开号：US20150336942A1

  公开（公告）日：2015-11-26

  The present invention is directed to aminopyridine derived compounds of formula (A). The compounds are considered useful for the treatment of diseases associated with LRRK2 such a Lewy body dementia, Parkinson's disease or cancer.

  本发明涉及公式（A）的氨基吡啶衍生物化合物。这些化合物被认为对于与LRRK2相关的疾病，如Lewy体痴呆、帕金森病或癌症的治疗是有用的。
• FUSED HETEROARYL MODULATORS OF GLUCOCORTICOID RECEPTOR, AP-1, AND/OR NF-kappaB ACTIVITY AND USE THEREOF
  申请人：Duan Jingwu

  公开号：US20110002952A1

  公开（公告）日：2011-01-06

  Novel non-steroidal compounds are provided which are useful in treating diseases or disorders associated with modulation of the glucocorticoid receptor, AP-1, and/or NF-κB activity, including metabolic and inflammatory and immune diseases or disorders, having the structure of formula (I): an enantiomer, diastereomer, or tautomer thereof, or a prodrug ester thereof, or a pharmaceutically-acceptable salt thereof, in which: Z is heterocyclo or heteroaryl; -A is a 5- to 8-membered carbocyclic ring or a 5- to 8-membered heterocyclic ring; B1 and B2 rings are pyridyl rings, wherein the B1 and B 2 rings are each fused to the A ring and the B1 ring is optionally substituted by one to three groups which are the same or different and are independently selected from R 1 , R 2 , and R 4 , and the B2 ring is optionally substituted by one to three groups which are the same or different and are independently selected from R3, R 7 , and R 3 71, J 2 , and J3 are at each occurrence the same or different and are independently -AIQA2-; Q is a bond, O, S, S(0), or S(O)2; A1 and A2 are the same or different and are at each occurrence independently selected from a bond, C1-3 alkylene, substituted C 1-3 alkylene, C24 alkenylene, and substituted C24 alkenylene, provided that A 1 and A2 are chosen so that ring A is a 5- to 8-membered carbocyclic or heterocyclic ring; R 1 to R 11 are as defined herein.

  提供了一种新型的非类固醇化合物，其在治疗与糖皮质激素受体、AP-1和/或NF-κB活性调节相关的疾病或疾病中具有用途，包括代谢性、炎症和免疫性疾病或疾病，其具有以下结构（I）的对映体、顺反异构体或互变异构体，或其前药酯，或其药学上可接受的盐，其中：Z是杂环或杂环芳基；-A是5-至8-成员的碳环或5-至8-成员的杂环；B1和B2环是吡啶环，其中B1和B2环各与A环融合，B1环可选地被1至3个基取代，所述基是相同或不同的，且独立地从R1、R2和R4中选择，B2环可选地被1至3个基取代，所述基是相同或不同的，且独立地从R3、R7和R371、J2和J3中选择，每次出现时，J2和J3是相同或不同的，且独立地为-AIQA2-；Q是键，O、S、S（0）或S（O）2；A1和A2是相同或不同的，且每次出现时独立地从键、C1-3烷基、取代C1-3烷基、C24烯基和取代C24烯基中选择，前提是A1和A2被选择为环A是5-至8-成员的碳环或杂环；R1至R11如本文所定义。