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10-acetyl-5H-imidazo<1,2-a>indolo<3,2-e>pyrazin-4-one | 161801-94-1

中文名称
——
中文别名
——
英文名称
10-acetyl-5H-imidazo<1,2-a>indolo<3,2-e>pyrazin-4-one
英文别名
16-Acetyl-2,5,8,16-tetrazatetracyclo[7.7.0.02,6.010,15]hexadeca-1(9),3,5,10,12,14-hexaen-7-one
10-acetyl-5H-imidazo<1,2-a>indolo<3,2-e>pyrazin-4-one化学式
CAS
161801-94-1
化学式
C14H10N4O2
mdl
——
分子量
266.259
InChiKey
BCIQFYFRLLORQJ-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

物化性质

  • 密度:
    1.57±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    20
  • 可旋转键数:
    0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    68.9
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • DERIVES D'IMIDAZO [1,2-A]PYRAZINE-4-ONE/UTILES COMME ANTAGONISTES DES RECEPTEURS AMPA ET NMDA
    申请人:RHONE-POULENC RORER S.A.
    公开号:EP0708778B1
    公开(公告)日:1997-02-05
  • US5672705A
    申请人:——
    公开号:US5672705A
    公开(公告)日:1997-09-30
  • [EN] IMIDAZO(1,2-A)PYRAZIN-4-ONE DERIVATIVES FOR USE AS AMPA AND NMDA RECEPTOR ANTAGONISTS<br/>[FR] DERIVES D'IMIDAZO (1,2-A)PYRAZINE-4-ONE/UTILES COMME ANTAGONISTES DES RECEPTEURS AMPA ET NMDA
    申请人:RHONE-POULENC RORER S.A.
    公开号:WO1995002602A1
    公开(公告)日:1995-01-26
    (EN) Compounds of formula (I), wherein R is an oxygen or sulphur atom or an NH or N-alk radical, and each of R1 and R2, which are the same or different, is a hydrogen or halogen atom or an alkyl, alkoxy, amino, acylamino, -NH-CO-NH-Ar,-N=CH-N(alk)alk', nitro, cyano, phenyl, imidazolyl or SO3H radical, the preparation thereof, and drugs containing such compounds, are disclosed.(FR) Composés de formule (I) dans laquelle R représente un atome d'oxygène ou de soufre ou un radical NH ou N-alk, R1 et R2, identiques ou différents, représentent des atomes d'hydrogène ou d'halogène ou des radicaux alkyle, alcoxy, amino, acylamino, -NH-CO-NH-Ar, -N=CH-N(alk)alk', nitro, cyano, phényle, imidazolyle ou SO3H, leur préparation et les médicaments les contenant.
  • An Efficient Preparative Route to Fused Imidazo[1,2-a]pyrazin-4-one Derivatives
    作者:Serge Mignani、Dominique Damour、Jean-Claude Aloup、Michel Barreau、Arielle Genevois-Borella、Patrick Jimonet、Jean-Pierre Leconte、Yves Ribeill、Marc Vuilhorgne
    DOI:10.3987/com-98-s(h)37
    日期:——
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同类化合物

咪唑并[1,2-a]噻吩并[3,2-E]吡嗪-5(4H)-酮 8-羟基咪唑并[1,2-a]吡嗪 5H,10H-二咪唑并[1,2-a:1,2-d]吡嗪-5,10-二酮 5H,10H-二咪唑并[1,2-a:1',5'-d]吡嗪-5,10-二酮 5,6,7,8-四氢-4H-环戊二烯并[E]咪唑并[1,2-a]吡嗪-4-酮 8-(3-benzylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 8-(3-butylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 8-(3-isopropylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 2-nitroimidazo[1,2-a]pyrazin-8(7H)-one 8-(4-methylpentanoyl)amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 3-(10-methyl-4,5-dihydro-4-oxo-10H-imidazo-[1,2-a]indeno[1,2-e]pyrazin-10-yl)propionitrile 10-[(1-methylimidazol-5-yl)methylene]-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one hydrochloride 8-(3-tert-butylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 8-(3-methylthioureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 10-formamido-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one 10-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one hydrochloride 8-hydroxy-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 8-Methoxy-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one 8-[3-morpholinoureido]-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazine-4-one hydrate 7-chloro-10-methylamino-5H,10H-imidazo-[1,2-a]indeno[1,2-e]pyrazin-4-one hydrochloride 7-chloro-10-formamido-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 10-acetamido-7-chloro-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 10-(2-pyridylmethyl)-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one 10-(4-imidazolylmethyl)-5H,10H-imidazo[1,2-a]-indeno[1,2-e]pyrazin-4-one 10-(pyridin-2-ylmethylene)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 10-(4-imidazolylmethylene)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 5H,10H-8-aminoimidazo[1,2-a]indeno[1,2-e]pyrazine-4-one monohydrochloride 10-(carboxymethylene)-8-(3-methylureido)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 8-amino-10-(carboxymethylene)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one dihydrochloride 8-ureido-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-4-one [4,5-dihydro-4-oxo-10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-8-yl]acetic acid 10-(2-methyl-1-propenyl)-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one RPR 119990 3-(9-carboxymethyl-4-oxo-5,10-dihydroimidazo[1,2-a]indeno[1,2-e]pyrazin-2-yl]propionic acid 10-[4-(imidazol-1-yl)butyl]-10-methyl-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 12-Methyl-3-thia-1,7,10-triazatricyclo[7.3.0.02,6]dodeca-2(6),4,9,11-tetraen-8-one 3-bromo-7-methyl-imidazo[1,2-a]pyrazin-8-one 5-chloro-7-methyl-8-oxo-6-phenyl-7,8-dihydroimidazo[1,2-a]-pyrazine-3-carbaldehyde ethyl 9-(diethoxyphosphorylmethyl)-4-oxo-5,10-dihydroimidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate ethyl 8-fluoro-4-oxo-4,5-dihydro-10H-imidazo[1,2-a]indeno[1,2-e]pyrazine-2-carboxylate 2-methyl-7H-imidazo[1,2-a]pyrazin-8-one 2-Methyl-7-[(1-phenylcyclopropyl)methyl]imidazo[1,2-a]pyrazin-8-one 3-bromo-2-methyl-7-(1-phenyl-cyclopropylmethyl)-7H-imidazo[1,2-a]pyrazin-8-one 5-chloro-7-(4-methoxybenzyl)-8-oxo-7,8-dihydroimidazo[1,2-a]-pyrazine-3-carbaldehyde 10-hydroxymethylene-5H,10H-imidazo[1,2-a]indeno[1,2-e]pyrazin-4-one 10-(carboxymethylene)-5H,10H-imidazo[1,2-a]indeno-[1,2-e]pyrazin-4-one 10-(carboxymethyl)-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one 8-oxo-7,8-dihydroimidazo[1,2-a]pyrazine hydrochloride 10-amino-5H,10H-imidazo[1,2-a]indeno[1,2-e]-pyrazin-4-one 10-(4-phenylbutyramido)-5H,10H-imidazo[1,2-a]-indeno[1,2-e]pyrazin-4-one