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3-碘-1-(四氢-2H-吡喃-2-基)-1H-吡唑并[4,3-B]吡啶 | 1562995-68-9

中文名称
3-碘-1-(四氢-2H-吡喃-2-基)-1H-吡唑并[4,3-B]吡啶
中文别名
——
英文名称
3-iodo-1-(tetrahydro-2H-pyran-2-yl)-1H-pyrazolo[4,3-b]pyridine
英文别名
3-iodo-1-(oxan-2-yl)pyrazolo[4,3-b]pyridine
3-碘-1-(四氢-2H-吡喃-2-基)-1H-吡唑并[4,3-B]吡啶化学式
CAS
1562995-68-9
化学式
C11H12IN3O
mdl
——
分子量
329.14
InChiKey
QHHOJYBMAQHTTB-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:
    438.6±45.0 °C(Predicted)
  • 密度:
    1.95±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    39.9
  • 氢给体数:
    0
  • 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

  • 4-HETEROARYL SUBSTITUTED BENZOIC ACID COMPOUNDS AS RORgammaT INHIBITORS AND USES THEREOF
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20150218096A1
    公开(公告)日:2015-08-06
    The present invention relates to compounds according to Formula I (Formula I), and pharmaceutically acceptable salts or solvates thereof. Such compounds can be used in the treatment of RORgammaT-mediated diseases or conditions.
    本发明涉及公式I(公式I)的化合物及其药学上可接受的盐或溶剂。这样的化合物可用于治疗RORgammaT介导的疾病或症状。
  • 4-heteroaryl substituted benzoic acid compounds as RORgammaT inhibitors and uses thereof
    申请人:Merck Sharp & Dohme Corp.
    公开号:US10196354B2
    公开(公告)日:2019-02-05
    The present invention relates to compounds according to Formula I (Formula I), and pharmaceutically acceptable salts or solvates thereof. Such compounds can be used in the treatment of RORgammaT-mediated diseases or conditions.
    本发明涉及根据式 I(式 I)的化合物及其药学上可接受的盐或溶液。此类化合物可用于治疗 RORgammaT 介导的疾病或病症。
  • Heteroaryl substituted benzoic acids as RORgammaT inhibitors and uses thereof
    申请人:Merck Sharp & Dohme Corp.
    公开号:US10584121B2
    公开(公告)日:2020-03-10
    The present invention relates to compounds according to Formula I and pharmaceutically acceptable salts thereof. Such compounds can be used in the treatment of RORgammaT-mediated diseases or conditions.
    本发明涉及根据式 I 的化合物及其药学上可接受的盐类。此类化合物可用于治疗 RORgammaT 介导的疾病或病症。
  • HETEROARYL SUBSTITUTED BENZOIC ACIDS AS RORGAMMAT INHIBITORS AND USES THEREOF
    申请人:Merck Sharp & Dohme Corp.
    公开号:EP3368535B1
    公开(公告)日:2020-12-02
  • HETEROARYL SUBSTITUTED BENZOIC ACIDS AS RORgammaT INHIBITORS AND USES THEREOF
    申请人:Merck Sharp & Dohme Corp.
    公开号:US20190194186A1
    公开(公告)日:2019-06-27
    The present invention relates to compounds according to Formula I and pharmaceutically acceptable salts thereof. Such compounds can be used in the treatment of RORgammaT-mediated diseases or conditions.
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溴代双满 6-硝基-2,4-二氢吡唑并[4,3-c]吡唑-3-羧酸 6-甲基-4-(三氟甲基)-1,6-二氢吡唑并[3,4-c]吡唑-3-基胺 5-(溴甲基)-N,N,N,2,6-五甲基-1,7-二氧代-1H,7H-吡唑并[1,2-A]吡唑-3-甲基溴化铵 3-碘-1-(四氢-2H-吡喃-2-基)-1H-吡唑并[4,3-B]吡啶 3-硝基-1,4-二氢吡唑并[4,3-c]吡唑 3-(溴甲基)-2,6,7-三甲基-1H,5H-吡唑并[1,2-a]吡唑-1,5-二酮 3,5-双溴甲基-2,6-二甲基吡唑并[1,2-a]吡唑-1,7-二酮 2,3,6-三甲基-5-[(2-吡啶基二硫代)甲基]-1H,7H-吡唑并[1,2-a]吡唑-1,7-二酮 2,3,6,7-四甲基-1,5-二氮杂双环[3.3.0]-2,6-辛二烯-4,8-二酮 2,3,5,6-四甲基-1H,7H-吡唑并[1,2-a]吡唑-1,7-二酮 9,10-dioxa-μ-methylthianio-syn-(methylene,methyl)bimane fluorosulfate 9,10-dioxa-anti-(bromomethyl,methyl)bimane 9,10-dioxa-syn-(hydrogen,bromo)bimane 9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 4,6-(1,4-tetramethylene)-3,7-dichloro-1,5-diazabicyclo<3.3.0>octa-3,6-diene-2,8-dione 9,10-dioxa-syn-(1-propylthiomethyl,methyl)bimane 9,10-dioxa-μ-tert-butylimino-syn-(methylene,methyl)bimane 9,10-dioxa-anti-(methyl,methyl)(methy,bromo)bimane 9,10-dioxa-syn-(fluoromethyl,methyl)(methyl,methyl)bimane 9,10-dioxa-syn-(trimethylammoniomethyl,methyl)(methyl,methyl)bimane bromide 9,10-dioxa-syn-(piperidinomethyl,methyl)bimane 9,10-dioxa-syn-(N-phenyl-N-methylaminomethyl,methyl)bimane 9,10-dioxa-syn-(trimethylammoniomethyl,methyl)bimane dibromide 9,10-dioxa-syn-(methylthiomethyl,methyl)bimane 9,10-dioxa-syn-(chloromethyl,methyl)bimane 9,10-dioxa-syn-(dimethylaminomethyl,methyl)bimane 9,10-dioxa-syn-(methoxymethyl,methyl)bimane (E)-1,4-dihydro-4-(nitromethylene)-1,2,5-trimethylpyridine syn-(methyl,hydro)(methyl,iodo)bimane 9,10-dioxa-μ-acetylimino-syn-(methylene,methyl)bimane 6,7-dihydro-5H-pyrazolo[1,2-a]pyrazol-4-ium-6-yl acetate;bromide 6-Chloro-1,2,5-trimethylpyrazolo[1,2-a]pyrazole-3,7-dione 3-Bromomethyl-5-hydroxymethyl-2,6-dimethyl-pyrazolo[1,2-a]pyrazole-1,7-dione syn-(methyl,iodo)bimane 1,7-bis(ethenyl)-2,6-dimethylpyrazolo[1,2-a]pyrazole-3,5-dione 9,10-dioxa-syn-(ethyl,chloro)bimane 9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 9,10-dioxa-anti-(hydroxymethyl,methyl)(methyl,methyl)bimane dl-9,10-dioxa-syn-(1-bromoethyl,methyl)bimane 1-(4-ethylsulfanyl-4H-pyridin-1-yl)-2,6-dimethylpyridin-4-one 3-Bromomethyl-5-ethyl-2,6-dimethyl-pyrazolo[1,2-a]pyrazole-1,7-dione 9,10-dioxa-anti-(chloromethyl,methyl)bimane 9,10-dioxa-μ-imino-syn-(methylene,methyl)bimane N,N-Dimethyl-2-nitro-2-(2H-tetrazol-5-yl)-1,1-ethenediamine 1-hydroxy-3,5-diiodo-4,6-dimethyl-1H-pyridin-2-one 9,10-dioxa-anti-(ethyl,chloro)bimane 2,6-dichloro-7-ethenyl-1-ethylpyrazolo[1,2-a]pyrazole-3,5-dione 2,6-dimethyl-3,5-dioxo-4,13-diazatricyclo[5.5.1.04,13]trideca-1,6-diene-10-carboxylic acid ethyl 2,6-dimethyl-3,5-dioxo-4,13-diazatricyclo[5.5.1.04,13]trideca-1,6-diene-10-carboxylate