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ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate | 365997-32-6

中文名称
——
中文别名
——
英文名称
ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate
英文别名
(1S,3R,4R)-3-azido-4-hydroxycyclohexanecarboxylic acidethyl ester;ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexanecarboxylate
ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate化学式
CAS
365997-32-6
化学式
C9H15N3O3
mdl
——
分子量
213.236
InChiKey
ZSEPOKOVRBPMOH-XLPZGREQSA-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):
    1.6
  • 重原子数:
    15
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    60.9
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:0d98b7afae0ab9aba5916b71b1eefddd
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反应信息

  • 作为反应物:
    描述:
    ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate2,2,6,6-四甲基哌啶氧化物磷酸吡哆醛碳酸氢钠异丙胺 、 sodium bromide 作用下, 以 aq. phosphate buffer 、 二氯甲烷 为溶剂, 生成 (1S,3R,4S)-4-amino-3-azidocyclohexane-1-carboxylic acid ethyl ester
    参考文献:
    名称:
    依度沙班中间体及其制备方法
    摘要:
    本发明公开了一种依度沙班中间体及其制备方法。依度沙班中间体的结构通式为 或 其中,R1为OH、烷氧基或N,N‑二烷基类基团,R2为氢、烷氧基羰基或氨基保护基。制备方法为:将 与氧化剂进行氧化反应得到式Ⅱ化合物;将式Ⅱ化合物、转氨酶、转氨酶辅酶及磷酸盐缓冲溶液混合进行酶催化反应或进一步经过胺基衍生化反应后,得到式Ⅰ化合物。与现有公开技术化学合成方法相比,本发明提供的这类依度沙班关键中间体及其制备方法具有结构新颖,反应条件温和,收率高,具有良好的工业化价值。
    公开号:
    CN115594613A
  • 作为产物:
    描述:
    (S)-(-)-3-环己烯甲酸N-溴代丁二酰亚胺(NBS) 、 potassium hydroxide 作用下, 以 乙醇 为溶剂, 反应 4.0h, 生成 ethyl (1S,3R,4R)-3-azido-4-hydroxycyclohexane-1-carboxylate
    参考文献:
    名称:
    依度沙班中间体及其制备方法
    摘要:
    本发明公开了一种依度沙班中间体及其制备方法。依度沙班中间体的结构通式为 或 其中,R1为OH、烷氧基或N,N‑二烷基类基团,R2为氢、烷氧基羰基或氨基保护基。制备方法为:将 与氧化剂进行氧化反应得到式Ⅱ化合物;将式Ⅱ化合物、转氨酶、转氨酶辅酶及磷酸盐缓冲溶液混合进行酶催化反应或进一步经过胺基衍生化反应后,得到式Ⅰ化合物。与现有公开技术化学合成方法相比,本发明提供的这类依度沙班关键中间体及其制备方法具有结构新颖,反应条件温和,收率高,具有良好的工业化价值。
    公开号:
    CN115594613A
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文献信息

  • Diamine derivatives
    申请人:Ohta Toshiharu
    公开号:US20050020645A1
    公开(公告)日:2005-01-27
    A compound represented by the general formula (1): Q 1 -Q 2 -T 0 -N(R 1 )-Q 3 -N(R 2 )-T 1 -Q 4 (1) wherein R 1 and R 2 are hydrogen atoms or the like; Q 1 is a saturated or unsaturated, 5- or 6-membered cyclic hydrocarbon group which may be substituted, or the like; Q 2 is a single bond or the like; Q 3 is a group in which Q 5 is an alkylene group having 1 to 8 carbon atoms, or the like; and T 0 and T 1 are carbonyl groups or the like; a salt thereof, a solvate thereof, or an N-oxide thereof. The compound is useful as an agent for preventing and/or treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.
    通用式(1)表示的化合物: Q1-Q2-T0-N(R1)-Q3-N(R2)-T1-Q4(1) 其中R1和R2是氢原子或类似物;Q1是饱和或不饱和的、5-或6-成员环烃基,可以被取代,或类似物;Q2是单键或类似物;Q3是一个基团,其中Q5是具有1至8个碳原子的烷基基团,或类似物;T0和T1是羰基团或类似物;其盐、溶剂合物或N-氧化物。 该化合物可用作预防和/或治疗脑梗死、脑栓塞、心肌梗死、心绞痛、肺梗死、肺栓塞、布尔格病、深静脉血栓形成、弥散性血管内凝血综合征、瓣膜或关节置换后的血栓形成、血管成形术后的血栓形成和再闭塞、全身性炎症反应综合征(SIRS)、多器官功能障碍综合征(MODS)、体外循环期间的血栓形成,或抽血时的血液凝结。
  • INHIBITORS OF THE FIBROBLAST GROWTH FACTOR RECEPTOR
    申请人:Bifulco, Jr. Neil
    公开号:US20150119405A1
    公开(公告)日:2015-04-30
    Described herein are inhibitors of FGFR-4, pharmaceutical compositions including such compounds, and methods of using such compounds and compositions.
    本处描述的是FGFR-4的抑制剂,包括含有此类化合物的药物组合物,以及使用此类化合物和组合物的方法。
  • Diamine Derivatives
    申请人:Ohta Toshiharu
    公开号:US20110312990A1
    公开(公告)日:2011-12-22
    A compound represented by the general formula (1): -Q 1 -Q 2 -T 0 -N(R 1 )-Q 3 -N(R 2 )-T 1 -Q 4 (1) wherein R 1 and R 2 are hydrogen atoms or the like; Q 1 is a saturated or unsaturated, 5- or 6-membered cyclic hydrocarbon group which may be substituted, or the like; Q 2 is a single bond or the like; Q 3 is a group in which Q 5 is an alkylene group having 1 to 8 carbon atoms, or the like; and T 0 and T 1 are carbonyl groups or the like; a salt thereof, a solvate thereof, or an N-oxide thereof. The compound is useful as an agent for preventing and/or treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.
    化合物的一般式表示为(1):-Q1-Q2-T0-N(R1)-Q3-N(R2)-T1-Q4(1),其中R1和R2为氢原子或类似物;Q1为饱和或不饱和的5-或6-成员环烃基,可以是取代基或类似物;Q2为单键或类似物;Q3为其中Q5为1至8个碳原子的烷基或类似物的基团;T0和T1为羰基或类似物。该化合物及其盐、溶剂化物或N-氧化物可用于预防和/或治疗脑梗死、脑栓塞、心肌梗死、心绞痛、肺梗死、肺栓塞、布尔格病、深静脉血栓形成、弥散性血管内凝血综合征、瓣膜或关节置换后的血栓形成、血管成形术后的血栓形成和再闭塞、全身性炎症反应综合征(SIRS)、多器官功能障碍综合征(MODS)、体外循环期间的血栓形成或采血时的血液凝固。
  • DRUG COMPOSITIONS AND METHODS FOR PREVENTING AND TREATING THROMBOSIS OR EMBOLISM
    申请人:OHTA Toshiharu
    公开号:US20090281074A1
    公开(公告)日:2009-11-12
    Drug compositions containing a substituted diamine compound represented by formula (1): Q 1 -Q 2 -r-N(R 1 )-Q 3 -N(R 2 )  (1) wherein Q 3 represents the following group wherein Q 5 represents an alkylene group having 4 carbon atoms, R 3 represents a hydrogen atom, and R 4 represents a 3-6 membered heterocyclic group which may be substituted; are useful for preventing and/or treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after artificial valve or joint replacement, thrombus formation and reocclusion after angioplasty, systemic inflammatory response syndrome (SIRS), multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing.
    含有以下式子(1)所代表的取代二胺化合物的药物组合物: Q1-Q2-r-N(R1)-Q3-N(R2)  (1) 其中,Q3代表以下基团: 其中,Q5代表具有4个碳原子的烷基基团,R3代表氢原子,R4代表可取代的3-6环杂环基团; 该药物组合物对于预防和/或治疗脑梗死、脑栓塞、心肌梗死、心绞痛、肺梗死、肺栓塞、布尔格病、深静脉血栓形成、弥散性血管内凝血综合征、人工瓣膜或关节置换后的血栓形成、血管成形术后的血栓形成和再闭塞、全身性炎症反应综合征(SIRS)、多器官功能障碍综合征(MODS)、体外循环期间的血栓形成或采血时的血凝。
  • METHOD FOR TREATING THROMBOSIS OR EMBOLISM AND RELATED DISEASES
    申请人:Ohta Toshiharu
    公开号:US20100099660A1
    公开(公告)日:2010-04-22
    A method for treating cerebral infarction, cerebral embolism, myocardial infarction, angina pectoris, pulmonary infarction, pulmonary embolism, Buerger's disease, deep venous thrombosis, disseminated intravascular coagulation syndrome, thrombus formation after artificial valve or joint replacement, thrombus formation and reocclusion after angioplasty, multiple organ dysfunction syndrome (MODS), thrombus formation during extracorporeal circulation, or blood clotting upon blood drawing is provided. The method includes administration of an effective amount of a compound represented by formula (1):
    提供了一种治疗脑梗塞、脑栓塞、心肌梗死、心绞痛、肺梗塞、肺栓塞、布尔格病、深静脉血栓形成、弥散性血管内凝血综合征、人工瓣膜或关节置换后的血栓形成、血管成形术后的血栓形成和再闭塞、多器官功能障碍综合征(MODS)、体外循环期间的血栓形成或采血时的血液凝固的方法。该方法包括给予化合物(1)式所代表的有效量。
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