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2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-ol | 1309047-95-7

中文名称
——
中文别名
——
英文名称
2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-ol
英文别名
2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidine-4-ol;2-amino-3,5,7,8-tetrahydropyrano[4,3-d]pyrimidin-4-one
2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-ol化学式
CAS
1309047-95-7
化学式
C7H9N3O2
mdl
——
分子量
167.167
InChiKey
VWNZPXHTSQBFKJ-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

  • 沸点:
    370.3±52.0 °C(Predicted)
  • 密度:
    1.70±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    -1.6
  • 重原子数:
    12
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    76.7
  • 氢给体数:
    2
  • 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

  • 作为反应物:
    描述:
    2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-ol三氯氧磷 作用下, 以 1,4-二氧六环 为溶剂, 生成 (2R)-2-[(2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-yl)amino]hexan-1-ol
    参考文献:
    名称:
    [EN] DIHYDROPYRANOPYRIMIDINES FOR THE TREATMENT OF VIRAL INFECTIONS
    [FR] DIHYDROPYRANOPYRIMIDINES POUR LE TRAITEMENT D'INFECTIONS VIRALES
    摘要:
    本发明涉及二氢吡喃吡啶啉衍生物,其制备方法,药物组合物以及它们在治疗病毒感染中的应用。
    公开号:
    WO2018002319A1
  • 作为产物:
    描述:
    盐酸胍4-氧代四氢-2H-吡喃-3-羧酸甲酯sodium ethanolate 作用下, 以 乙醇 为溶剂, 反应 0.17h, 以81%的产率得到2-amino-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-4-ol
    参考文献:
    名称:
    [EN] DIHYDROPYRANOPYRIMIDINES FOR THE TREATMENT OF VIRAL INFECTIONS
    [FR] DIHYDROPYRANOPYRIMIDINES POUR LE TRAITEMENT D'INFECTIONS VIRALES
    摘要:
    本发明涉及二氢吡喃吡啶啉衍生物,其制备方法,药物组合物以及它们在治疗病毒感染中的应用。
    公开号:
    WO2018002319A1
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文献信息

  • Bicyclic pyrimidine compounds and therapeutic use thereof
    申请人:Sumitomo Pharmaceuticals Company, Limited
    公开号:US06458798B1
    公开(公告)日:2002-10-01
    A pyrimidine derivative of the formula (1) or a salt thereof; has an inhibitory activity of production of Th2 type cytokines such as IL-4, IL-5, etc., and is useful as an therapeutic agent for allergic diseases, autoimmune diseases such as systemic lupus erythemathosus, etc., and acquired immunodeficiecy syndrome (AIDS) and so on.
    公式(1)的嘧啶生物或其盐;具有抑制Th2型细胞因子(如IL-4、IL-5等)产生的活性,并且对过敏性疾病、系统性红斑狼疮等自身免疫疾病以及获得性免疫缺陷综合征(AIDS)等疾病具有治疗作用。
  • Pyrimidine derivative
    申请人:SUMITOMO PHARMACEUTICALS COMPANY LIMITED
    公开号:US20030105323A1
    公开(公告)日:2003-06-05
    1. A pyrimidine derivative of the formula (1) or a salt thereof; 1 has an inhibitory activity of production of Th2 type cytokines such as IL-4, IL-5, etc., and is useful as an therapeutic agent for allergic diseases, autoimmune diseases such as systemic lupus erythemathosus, etc., and acquired immunodeficiecy syndrome (AIDS) and so on.
    式(1)的嘧啶生物或其盐;具有抑制Th2型细胞因子如IL-4,IL-5等的产生的活性,可用作过敏疾病,自身免疫性疾病如系统性红斑狼疮等,以及获得性免疫缺陷综合症(AIDS)等治疗剂。
  • PYRIMIDINE DERIVATIVES
    申请人:Sumitomo Pharmaceuticals Company, Limited
    公开号:EP1110951A1
    公开(公告)日:2001-06-27
    1. A pyrimidine derivative of the formula (1) or a salt thereof; has an inhibitory activity of production of Th2 type cytokines such as IL-4, IL-5, etc., and is useful as an therapeutic agent for allergic diseases, autoimmune diseases such as systemic lupus erythemathosus, etc., and acquired immunodeficiecy syndrome (AIDS) and so on.
    1.式(1)的嘧啶生物或其盐; 具有抑制 IL-4、IL-5 等 Th2 型细胞因子产生的活性,可作为过敏性疾病、系统性红斑狼疮等自身免疫性疾病和获得性免疫缺陷综合征(艾滋病)等的治疗剂。
  • Dihydropyranopyrimidines for the treatment of viral infections
    申请人:Janssen Sciences Ireland Unlimited Company
    公开号:US11053256B2
    公开(公告)日:2021-07-06
    This invention relates to dihydropyranopynmidine derivatives, processes for their preparation, pharmaceutical compositions, and their use in treating viral infections.
    本发明涉及二氢喃炔脒衍生物、其制备工艺、药物组合物及其在治疗病毒感染中的用途。
  • 4 - PIPERIDINYL COMPOUNDS FOR USE AS TANKYRASE INHIBITORS
    申请人:Novartis AG
    公开号:EP2731940B1
    公开(公告)日:2015-08-19
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同类化合物

叔-丁基2-(甲磺酰)-5,7-二氢螺[吡喃并[4,3-D]嘧啶并-8,3-吡咯烷]-1-甲酸基酯 乙基7'-氨基-6-氟-2,2',4'-三羰基-1,1',2,2',3',4'-六氢螺[吲哚-3,5'-吡喃并[2,3-d]嘧啶]-6'-羧酸酯 7H-吡喃并[2,3-d]嘧啶-7-酮 7H-吡喃并[2,3-d]嘧啶 7,8-二氢-5H-吡喃并[4,3-D]嘧啶-2-胺 5H-吡喃并[4,3-d]嘧啶 5H-吡喃并[2,3-d]嘧啶 2H-吡喃并[2,3-d]嘧啶-6-甲腈,7-氨基-1,3,4,5-四氢-5-(4-甲氧苯基)-2,4-二羰基- 2,4-二氯-7,8-二氢-5H-吡喃[4,3-d]嘧啶 1H-吡喃并[3,4-d]嘧啶 1H-吡喃并[3,2-d]嘧啶 (5S,7R,8S)-2-methylsulfanyl-5,8-dihydro-7-allyloxymethyl-5-methoxy-pyrano[3,4-d]-pyrimidin-8-ol 5-ethyl-2-[(Z)-1-thiophen-3-ylpentylideneamino]oxy-3H-pyrano[2,3-d]pyrimidine-4,7-dione 5-ethyl-2-[[1-(3-methylbutanoyl)piperidin-4-ylidene]amino]oxy-3H-pyrano[2,3-d]pyrimidine-4,7-dione 5-butyl-2-[(E)-1-(4-cyclohexylpiperazin-1-yl)butylideneamino]oxy-3H-pyrano[2,3-d]pyrimidine-4,7-dione 2,3,3a,9-tetrahydro-5-iodo-2,3,3-trimethylimidazo[5,1-b][1,3]benzoxazin-1-one 2,4-dimethyl-9-methoxy-4,12b-dihydro-1H,7H-chromeno[4',3'-4,5]pyrano[2,3-d]pyrimidine-1,3(2H)-dione 5-methyl-3-{3-[(R)-2-oxo-3-(3-oxo-3,4-dihydro-2H-pyrido[3,2-b][1,4]oxazin-6-yl)-oxazolidin-5-yl]-propyl}-1H-quinazoline-2,4-dione 7-amino-2-(benzothiazol-2-ylmethyl)-9-phenylthiazolo[4',5':6,5]pyrano[2,3-d]pyrimidine-8(7H)-one 2-[6-[(2-chlorophenyl)methyl]pyridin-2-yl]-7,8-dihydro-5H-pyrano[4,3-d]pyrimidine 8-amino-2-(methylthio)-5-oxo-6-(pyridin-4-yl)-5,6-dihydro-4H-pyrano[2,3-d][1,3]thiazolo[4,5-b]pyridine-7-carbonitrile 5-(4-chlorophenyl)-1,3,8,8-tetramethyl-7,9-dihydro-5H-chromeno[2,3-d]pyrimidine-2,4,6-trione ethyl 7'-amino-2,4'-dioxo-2'-thioxo-1,1',2,2',3',4'-hexahydrospiroindole-3,5'-pyrano[2,3-d]pyrimidine-6'-carboxylate 8-amino-2-(methylthio)-5-oxo-6-(pyridin-3-yl)-5,6-dihydro-4H-pyrano[2,3-d][1,3]thiazolo[4,5-b]pyridine-7-carbonitrile 7-Amino-4-oxo-5-phenyl-2-thioxo-1,3,4,5-tetrahydro-2H-pyrano[2,3-d]pyrimidine-6-carboxylic acid ethyl ester 3-(1H-benzoimidazol-2-yl)-3-butyl-5-methyl-dihydro-furan-2-one 3-(1H-benzoimidazol-2-yl)-3-(2-diethylamino-ethyl)-5-methyl-dihydro-furan-2-one 1-{4-[(1R,9S)-3-((S)-3-methyl-morpholin-4-yl)-12-oxa-4,6-diaza-tricyclo[7.2.1.0-2,7]dodeca-2(7),3,5-trien-5-yl]-phenyl}-3-oxetan-3-yl-urea (S)-6-(4-(4-(3-ethylmorpholino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)phenylamino)pyridin-2(1H)-one 3-(1H-benzoimidazol-2-yl)-5-methyl-3-(3-methyl-butyl)-dihydro-furan-2-one 13-(3,4-dimethoxyphenyl)-5,5-dimethyl-2-thioxo-2,5,6,8,9,13-hexahydro-4H-pyrimido[5',4':6,7][1,8]naphthyridino[4,3,2-de]quinazoline-10,12(3a1H,11H)-dione (S)-3-allyl-8-ethyl-4,7-dioxo-2-(phenylcarbamoyl)-4,5,7,8-tetrahydro-3H-pyrano[4,3-d]pyrimidin-8-yl acetate 8-{[(2-bromo-3-methylphenyl)oxy]methyl}-1,3-dimethyl-2,3,4,6-tetrahydro-1H-pyrano[3,2-d]pyrimidine-2,4-dione 9-ethyl-6a-methyl-2-phenyl-8,9-dihydro-oxazolo[2,3-b]pyrimido[4,5-d][1,3]oxazin-5-one (S)-1-cyclobutyl-3-(4-(4-(3-methylmorpholino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)phenyl)urea (S)-2-(4-(4-(3-ethylmorpholino)-7,8-dihydro-5H-pyrano[4,3-d]pyrimidin-2-yl)phenylamino)pyrimidin-4(3H)-one (6aRS,10aRS)-4,6,6a,7,8,9,10,10a-octahydro-2,4,6,6-tetramethyl-1H-<2>benzopyrano<3,4-d>pyrimidine-1,3(2H)-dione 5-ethyl-2-[(E)-1-thiophen-3-ylpentylideneamino]oxy-3H-pyrano[2,3-d]pyrimidine-4,7-dione N3-(methyl 4-deoxy-α-L-threo-hex-4-enopyranosyluronate)-5-fluorouracil 1-{4-[(1S,9R)-3-((S)-3-methyl-morpholin-4-yl)-12-oxa-4,6-diaza-tricyclo[7.2.1.0-2,7]dodeca-2(7),3,5-trien-5-yl]-phenyl}-3-oxetan-3-yl-urea 4,5-dimethyl-12-(4-methoxyphenyl)-2-thioxo-2,4a,7,8,9,10,11,12-octahydrodipyrimido[4,5-b;4',5'-f] [1,8]naphthyridine-9,11-dione 2-[4-[2-hydroxyethyl(methyl)amino]-2-methyl-7-oxopyrimido[5,4-b][1,4]oxazin-8-yl]acetonitrile 5-ethyl-2-[(Z)-1-thiophen-2-ylethylideneamino]oxy-3H-pyrano[2,3-d]pyrimidine-4,7-dione