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5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde | 679840-18-7

中文名称
——
中文别名
——
英文名称
5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde
英文别名
5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-2,3-difluoro-benzaldehyde;5-acetyl-2-[(2S,6R)-2,6-dimethylmorpholin-4-yl]-3,4-difluorobenzaldehyde
5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde化学式
CAS
679840-18-7
化学式
C15H17F2NO3
mdl
——
分子量
297.302
InChiKey
FJAWWMXTWDVZEL-DTORHVGOSA-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

物化性质

  • 沸点:
    451.6±45.0 °C(Predicted)
  • 密度:
    1.216±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    46.6
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为反应物:
    描述:
    5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde 生成 rel-(2R,4S,4aS)-8-acetyl-9,10-difluoro-1,2,4,4a-tetrahydro-2,4-dimethylspiro[[1,4]oxazino[4,3-a]quinoline-5(6H),5'(2'H)-pyrimidine]-2',4',6'(1'H,3'H)-trione
    参考文献:
    名称:
    [EN] TRICYCLIC TETRAHYDROQUINOLINE ANTIBACTERIAL AGENTS
    [FR] AGENTS ANTI-BACTERIENS A BASE DE TETRAHYDROQUINOLINE TRICYCLIQUE
    摘要:
    该发明包括式(I)的四氢喹啉及相关化合物,以及展现出对广泛的人类和兽医病原体具有有用抗菌活性的药物组合物。
    公开号:
    WO2004031195A1
  • 作为产物:
    描述:
    1-[4-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-2,3-difluoro-5-hydroxymethyl-phenyl]-ethanone 在 四丙基高钌酸铵N-甲基吗啉氧化物 作用下, 以 二氯甲烷乙腈 为溶剂, 以94%的产率得到5-acetyl-2-((2R,6S)-2,6-dimethyl-morpholin-4-yl)-3,4-difluoro-benzaldehyde
    参考文献:
    名称:
    [EN] FUSED, SPIROCYCLIC HETEROAROMATIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS
    [FR] COMPOSÉS HÉTÉROAROMATIQUES SPIROCYCLIQUES FUSIONNÉS POUR TRAITER LES INFECTIONS BACTÉRIENNES
    摘要:
    本发明涉及式(I)的化合物;其药学上可接受的盐;使用它们治疗细菌感染的方法;以及它们的制备方法。
    公开号:
    WO2010043893A1
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文献信息

  • TRICYCLIC TETRAHYDROQUINOLINE ANTIBACTERIAL AGENTS
    申请人:Barbachyn Michael Robert
    公开号:US20100022524A1
    公开(公告)日:2010-01-28
    The invention includes tetrahydroquinoline and related compounds of formula I, and pharmaceutical compositions thereof, that exhibit useful antibacterial activity against a wide range of human and veterinary pathogens.
    该发明涉及公式I的四氢喹啉及相关化合物,以及其制备的药物组合物,对于广泛的人类和兽医病原体具有有用的抗菌活性。
  • Tricyclic tetrahydroquinoline antibacterial agents
    申请人:Barbachyn Robert Michael
    公开号:US20070161630A1
    公开(公告)日:2007-07-12
    The invention includes tetrahydroquinoline and related compounds of formula I, and pharmaceutical compositions thereof, that exhibit useful antibacterial activity against a wide range of human and veterinary pathogens.
    本发明涉及公式I的四氢喹啉及其相关化合物,以及具有对广泛的人类和兽医病原体有用的抗菌活性的制药组合物。
  • Tricyclic Tetrahydroquinoline Antibacterial Agents
    申请人:Barbachyn Michael Robert
    公开号:US20110092494A1
    公开(公告)日:2011-04-21
    The invention includes tetrahydroquinoline and related compounds of formula I, and pharmaceutical compositions thereof, that exhibit useful antibacterial activity against a wide range of human and veterinary pathogens.
    该发明涉及公式I的四氢喹啉及相关化合物,以及其制备的药物组合物,对人类和兽医病原体具有有用的抗菌活性。
  • CHEMICAL COMPOUNDS
    申请人:Basarab Gregory Steven
    公开号:US20100261719A1
    公开(公告)日:2010-10-14
    In one aspect, the present invention relates to compounds of Formula (I) and to pharmaceutically acceptable salts thereof, wherein: n is 1 to 4; and R 3 in each occurrence is independently selected from —X—R 5 , —W—R 6 , —C(O)—N(R 3a )—S(O) 2 —R 3b , —C(R 3a )═N—R 3y , C(R 3a )═N—N(R 3a )—C(O)—R 3b , C(R 3a )═N—N(R 3a )—C(O) 2 —R 3b , —C(R 3a )═N—N(R 3y ) 2 , —C(R 3a )═N—N(R 3a )—C(O)—N(R 3y ) 2 , —C(NR 3a ) 2 )═N—R 3y , —C(N(R 3a ) 2 )═N—OR 3y , —C(N(R 3a ) 2 )═N—C(O)—R 3b , —C(N(R 3a ) 2 ═N—S(0) 2 —R 3b , —C(N(R 3a ) 2 )═N—CN, —N═C(R 3y ) 2 , —N(R 3a )—S(O) 2 —N(R 3y ) 2 , —N(R 3a )—N(R 3y 2 , —N(R 3a )—C(O)—N(R 3y ) 2 , —N(R 3a )—C(O)—N(R 3a )—S(O) 2 —R 3b , —N(R 3a )—C(R 3a )═N(R 3y ), —N(R 3a )—C(R 3a )═N—OR 3y , —N(R 3a )—C(R 3a )═N—C(O)—R 3b , —N(R 3a )—C(R 3a )═N—S(O) 2 R— 3b , —N(R 3a )—C(R 3a )═N—CN, —N(R 3a )—C(N(R 3a ) 2 )═N—R 3y , —N(R 3a )—C(N(R 3a ) 2 )═N—OR 3y , —N(R 3a )—C(N(R 3a ) 2 )═N—C(O)—R 3b , —N(R 3a )—C(N(R 3a ) 2 )—N—S(O) 2 —R 3b , —N(R 3a )—C(N(R 3a ) 2 )—N—CN, —O—C(O)—R 3 , and —Si(R 3b ) 3 ; to methods of using them to treat bacterial infections, and to methods for their preparation.
    在一方面,本发明涉及公式(I)的化合物及其药学上可接受的盐,其中:n为1到4;每次R3独立地选择自—X—R5,—W—R6,—C(O)—N(R3a)—S(O)2—R3b,—C(R3a)═N—R3y,C(R3a)═N—N(R3a)—C(O)—R3b,C(R3a)═N—N(R3a)—C(O)2—R3b,—C(R3a)═N—N(R3y)2,—C(R3a)═N—N(R3a)—C(O)—N(R3y)2,—C(NR3a)2)═N—R3y,—C(N(R3a)2)═N—OR3y,—C(N(R3a)2)═N—C(O)—R3b,—C(N(R3a)2═N—S(0)2—R3b,—C(N(R3a)2)═N—CN,—N═C(R3y)2,—N(R3a)—S(O)2—N(R3y)2,—N(R3a)—N(R3y2,—N(R3a)—C(O)—N(R3y)2,—N(R3a)—C(O)—N(R3a)—S(O)2—R3b,—N(R3a)—C(R3a)═N(R3y),—N(R3a)—C(R3a)═N—OR3y,—N(R3a)—C(R3a)═N—C(O)—R3b,—N(R3a)—C(R3a)═N—S(O)2R—3b,—N(R3a)—C(R3a)═N—CN,—N(R3a)—C(N(R3a)2)═N—R3y,—N(R3a)—C(N(R3a)2)═N—OR3y,—N(R3a)—C(N(R3a)2)═N—C(O)—R3b,—N(R3a)—C(N(R3a)2)—N—S(O)2—R3b,—N(R3a)—C(N(R3a)2)—N—CN,—O—C(O)—R3,和—Si(R3b)3;以及使用它们治疗细菌感染的方法和它们的制备方法。
  • FUSED, SPIROCYCLIC HETEROAROMATIC COMPOUNDS FOR THE TREATMENT OF BACTERIAL INFECTIONS
    申请人:Barvian Kevin
    公开号:US20110245224A1
    公开(公告)日:2011-10-06
    The present invention relates to compounds of Formula (I); to pharmaceutically acceptable salts thereof, to methods of using them to treat bacterial infections, and to methods for their preparation.
    本发明涉及式(I)的化合物;其药学上可接受的盐;使用它们治疗细菌感染的方法;以及它们的制备方法。
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