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N-[6-氯-5-(2-甲氧基苯氧基)[2,2’-联嘧啶]-4-基]-4-叔丁基苯磺酰胺钾盐 | 301646-59-3

中文名称
N-[6-氯-5-(2-甲氧基苯氧基)[2,2’-联嘧啶]-4-基]-4-叔丁基苯磺酰胺钾盐
中文别名
N-[6-氯-5-(2-甲氧基苯氧基)[2,2’-联嘧啶]-4-基]-4-叔丁基苯磺酰胺钾盐;N-[6-氯-5-(2-甲氧基苯氧基)[2,2`-联嘧啶]-4-基]-4-叔丁基苯磺酰胺钾盐;N-[6-氯-5-(2-甲氧基苯氧基)[2,2'-联嘧啶]-4-基]-4-叔丁基苯磺酰胺钾盐
英文名称
4-tert-butyl-N-[6-chloro-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]benzene sulfonamide potassium salt
英文别名
4-(tert-butyl)-N-(6-chloro-5-(2-methoxyphenoxy)-(2,2'-bipyrimidin)-4-yl)benzenesulfonamide potassium salt;p-tert-butyl-N-[6-chloro-5-(2-methoxy-phenoxy)-[2,2'-bipyrimidin]-4-yl]benzenesulfonamide potassium salt;4-tert-butyl-N-[6-chloro-5-(2-methoxy-phenoxy)-2-(2-pyrimidinyl)-pyrimidin-4-yl]-benzenesulfonamide potassium salt;Potassium ((4-(tert-butyl)phenyl)sulfonyl)(6-chloro-5-(2-methoxyphenoxy)-[2,2'-bipyrimidin]-4-yl)amide;potassium;(4-tert-butylphenyl)sulfonyl-[6-chloro-5-(2-methoxyphenoxy)-2-pyrimidin-2-ylpyrimidin-4-yl]azanide
N-[6-氯-5-(2-甲氧基苯氧基)[2,2’-联嘧啶]-4-基]-4-叔丁基苯磺酰胺钾盐化学式
CAS
301646-59-3
化学式
C25H23ClN5O4S*K
mdl
——
分子量
564.106
InChiKey
AKVKGLFONGGDDC-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    3.08
  • 重原子数:
    37
  • 可旋转键数:
    8
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.2
  • 拓扑面积:
    114
  • 氢给体数:
    0
  • 氢受体数:
    9

安全信息

  • 储存条件:
    室温

反应信息

点击查看最新优质反应信息

文献信息

  • PROCESS FOR THE PREPARATION OF BOSENTAN MONOHYDRATE
    申请人:Kompella Amala Kishan
    公开号:US20130245259A1
    公开(公告)日:2013-09-19
    The invention relates to improved processes for the preparation of bosentan monohydrate which provide higher yield and purity.
    这项发明涉及改进的制备博瑟坦单合物的工艺,可提供更高的产量和纯度。
  • 보센탄 일수화물의 제조방법, 이에 사용되는 신규 중간체 및 이의 제조방법
    申请人:JEIL PHARMACEUTICAL CO.,LTD 제일약품주식회사(120170326287) Corp. No ▼ 110111-6420361BRN ▼628-88-00669
    公开号:KR102004422B1
    公开(公告)日:2019-07-26
    본 발명은 보센탄 일수화물의 제조방법, 이에 사용되는 신규 중간체 화합물 및 이의 제조방법을 제공한다. 본 발명의 신규 중간체 화합물은 고수율 및 고순도로 제조되며, 이를 이용하여 고순도의 보센탄 일수화물을 고수율로 경제적으로 대량생산할 수 있다.
    该专利提供了一种制备烷烃类化合物的方法,以及用于该方法的新型中间体化合物及其制备方法。该专利的新型中间体化合物经过高产率和高纯度制备,利用这些化合物可以经济地大规模生产高纯度的烷烃类化合物。
  • PROCESS FOR PREPARATION OF ENDOTHELIAL RECEPTOR ANTAGONIST (BOSENTAN)
    申请人:Joshi Shreerang
    公开号:US20120136015A1
    公开(公告)日:2012-05-31
    The present invention relates to processes for the preparation of an endothelial receptor antagonist. The present invention particularly relates to synthesis of 4-tert-butyl-N-[6-(2-hydroxyethoxy)-5-(2-methoxyphenoxy)-2-(2-pyrimidinyl)-4-pyrimidinyl]benzene sulfonamide (bosentan).
    本发明涉及制备内皮受体拮抗剂的方法。本发明特别涉及4-叔丁基-N-[6-(2-羟基乙氧基)-5-(2-甲氧基苯氧基)-2-(2-嘧啶基)-4-嘧啶基]苯磺酰胺(博生坦)的合成。
  • [EN] METHOD OF SYNTHESIS OF BOSENTAN, ITS POLYMORPHIC FORMS AND ITS SALTS<br/>[FR] PROCÉDÉ DE SYNTHÈSE DU BOSENTAN, DE SES FORMES POLYMORPHIQUES ET DE SES SELS
    申请人:CIPLA LTD
    公开号:WO2009083739A1
    公开(公告)日:2009-07-09
    The present invention relates to alkaline earth metal salts of bosentan, anhydrous bosentan, polymorphic forms thereof, amorphous bosentan and processes for preparing them. The present invention further relates to a process for the preparation of bosentan and its pharmaceutically acceptable salts.
    本发明涉及波生坦的碱土属盐、无波生坦、其多形态形式、无定形波生坦以及制备它们的工艺。本发明还涉及一种制备波生坦及其药用可接受盐的方法。
  • Research and Development of a Second-Generation Process for Bosentan, an Endothelin Receptor Antagonist
    作者:Peter J. Harrington、Hiralal N. Khatri、Brad S. DeHoff、Martin R. Guinn、Mark A. Boehler、Karl A. Glaser
    DOI:10.1021/op010234i
    日期:2002.3.1
    A second-generation manufacturing process from 5-(2-methoxyphenoxy)-[2,2'-bipyrimidine]-4,6-(1H,5H)-dione to bosentan is based on the synthesis and deprotection of the tert-butyl ether of bosentan using available and inexpensive ethylene glycol mono-tert-butyl ether. This new strategy triggered a cascade of process improvements. Isolations are reduced from six to three, and drying operations, from five to two. Process solvents are reduced from six to two. The isolations of two sensitizers are eliminated. Toluene is used in place of methylene chloride. Two aqueous waste streams are eliminated by replacing DMF and ethylene glycol by toluene. Two methanol-isopropyl acetate recrystallizations of bosentan are replaced by the decantation of a suspension of bosentan formate monoethanolate in ethanol-toluene. Finally, the overall yield is increased from 67 to 84% and the final product purity improved from 99.3 to 99.7%.
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