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3-ethoxy-4-(ethoxycarbonyl)-benzoic acid

中文名称
——
中文别名
——
英文名称
3-ethoxy-4-(ethoxycarbonyl)-benzoic acid
英文别名
3-Ethoxy-4-(Ethoxycarbonyl)Benzoic Acid;3-ethoxy-4-ethoxycarbonylbenzoic acid
3-ethoxy-4-(ethoxycarbonyl)-benzoic acid化学式
CAS
——
化学式
C12H14O5
mdl
——
分子量
238.24
InChiKey
YWPBMZGQYGVLKL-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

计算性质

  • 辛醇/水分配系数(LogP):
    1.9
  • 重原子数:
    17
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    72.8
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    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:
    3-ethoxy-4-(ethoxycarbonyl)-benzoic acid盐酸 、 lithium hydroxide monohydrate 、 1-羟基苯并三唑盐酸-N-乙基-Nˊ-(3-二甲氨基丙基)碳二亚胺N,N-二异丙基乙胺 、 sodium hydroxide 作用下, 以 四氢呋喃甲醇乙醚二氯甲烷乙酸乙酯 为溶剂, 反应 49.0h, 生成 4-(3-oxa-8-azabicyclo[3.2.1]octane-8-carbonyl)-2-ethoxy-N-((R)-2-hydroxy-2-((S)-1,2,3,4-tetrahydroisoquinolin-3-yl)ethyl)benzamide
    参考文献:
    名称:
    [EN] TETRAHYDROISOQUINOLINES AS PRMT5 INHIBITORS
    [FR] TÉTRAHYDRO-ISOQUINOLÉINES EN TANT QU'INHIBITEURS DE PRMT5
    摘要:
    式(I)的化合物中:n为1或2;p为0或1;R1a、R1b、R1c和R1d分别独立地选自H、卤素、C1-4烷氧基、C1-4烷基、C1-4氟烷基、C3-4环烷基、NH-C1-4烷基和氰基组成的群;R2a和R2b分别独立地选自以下组成的群:(i)F;(ii)H;(iii)Me;和(iv)CH2OH;R2c和R2d分别独立地选自以下组成的群:(i)F;(ii)H;(iii)Me;和(iv)CH2OH;R2e为H或Me;R3a和R3b分别独立地选自H和Me;R4为H或Me;R5为H或Me;R6a和R6b分别独立地选自H和Me;A为(i)可选择地取代的苯基;(ii)可选择地取代的萘基;或(iii)可选择地取代的C5-12杂环芳基;其中当R2e为H时,至少有一个R1a、R1b、R1c和R1d选自C1-4烷氧基、C2-4烷基、C1-4氟烷基、C3-4环烷基、NH-C1-4烷基和氰基。
    公开号:
    WO2017153513A1
  • 作为产物:
    描述:
    参考文献:
    名称:
    [EN] TETRAHYDROISOQUINOLINE DERIVED PRMT5-INHIBITORS
    [FR] INHIBITEURS DE PRMT5 DÉRIVÉS DE TÉTRAHYDROISOQUINOLÉINE
    摘要:
    式I的化合物,其中:n为1或2;p为0或1;R1可选地为一个或多个卤素或甲基基团;R2a和R2b分别选自以下组:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R2c和R2d分别选自以下组:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R3a和R3b分别选自H和Me;R4为H或Me;R5为H或Me;R6a和R6b分别选自H和Me;A为(i)可选地取代的苯基;(ii)可选地取代的萘基;或(iii)可选地取代的C5-12杂环基。
    公开号:
    WO2016034673A1
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文献信息

  • [EN] TETRAHYDROISOQUINOLINE DERIVED PRMT5-INHIBITORS<br/>[FR] INHIBITEURS DE PRMT5 DÉRIVÉS DE TÉTRAHYDROISOQUINOLÉINE
    申请人:CTXT PTY LTD
    公开号:WO2016034673A1
    公开(公告)日:2016-03-10
    A compound of formula I wherein: n is 1 or 2: p is 0 or 1; R1 is optionally one or more halo or methyl groups; R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2c and R2d are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R3a and R3b are independently selected from H and Me; R4 is either H or Me; R5 is either H or Me; R6a and R6b are independently selected from H and Me; A is either (i) optionally substituted phenyl; (ii) optionally substituted naphthyl; or (iii) optionally substituted C5-12 heteroaryl.
    式I的化合物,其中:n为1或2;p为0或1;R1可选地为一个或多个卤素或甲基基团;R2a和R2b分别选自以下组:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R2c和R2d分别选自以下组:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R3a和R3b分别选自H和Me;R4为H或Me;R5为H或Me;R6a和R6b分别选自H和Me;A为(i)可选地取代的苯基;(ii)可选地取代的萘基;或(iii)可选地取代的C5-12杂环基。
  • [EN] 3-OXA-8-AZABICYCLO[3.2.1]OCTANE DERIVATIVES AND THIER USE IN THE TREATMENT OF CANCER AND HEMOGLOBINOPATHIES<br/>[FR] DÉRIVÉS DE 3-OXA-8-AZABICYCLO [3.2.1] OCTANE ET LEUR UTILISATION DANS LE TRAITEMENT DU CANCER ET D'HÉMOGLOBINOPATHIES
    申请人:CTXT PTY LTD
    公开号:WO2017153519A1
    公开(公告)日:2017-09-14
    A compound of formula Ia, Ib, Ic or Id: wherein: n is 1 or 2;R N is H or Me; R1 is optionally one or more halo or methyl groups;R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H;(iii) Me; and (iv) CH2 OH; R 2c and R 2d (if present) are independently selected from the group consisting of: (i) F; (ii) H;(iii) Me; and(iv) CH 2 OH;R 3a and R 3b are independently selected from H and Me; R 4a is selected from OH,-NH 2, -C(=O)NH 2, and -CH 2 OH; R 4b is either H or Me; R5 is either H or Me; m is 1 or 2; q is 0 or 1;R 11a, R 11b, R 11c and R 11d are independently selected from H, halo, C1-4 alkyl, C 1-4 fluoroalkyl, C 3-4 cycloalkyl, C 1-4 alkyloxy, NH-C 1-4 alkyl and cyano; R 12a and R 12b are independently selected from the group consisting of: (i) F; (ii) H;(iii) Me; and (iv) CH 2 OH; R 12c and R 12d are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH 2 OH;R 12e is H or Me; R 13a and R 13b are independently selected from H and Me; R 14 is either H or Me; R 16a and R 16b are independently selected from H and Me; R 6 is selected from H, OMe, and OEt.
    公式Ia、Ib、Ic或Id的化合物:其中:n为1或2;RN为H或Me;R1是可选的一个或多个卤素或甲基基团;R2a和R2b分别选自以下群体中的一种:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R2c和R2d(如果存在)分别选自以下群体中的一种:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R3a和R3b分别选自H和Me;R4a选自OH、-NH2、-C(=O)NH2和-CH2OH;R4b为H或Me;R5为H或Me;m为1或2;q为0或1;R11a、R11b、R11c和R11d分别选自H、卤素、C1-4烷基、C1-4氟代烷基、C3-4环烷基、C1-4烷氧基、NH-C1-4烷基和氰基;R12a和R12b分别选自以下群体中的一种:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R12c和R12d分别选自以下群体中的一种:(i) F;(ii) H;(iii) Me;和(iv) CH2OH;R12e为H或Me;R13a和R13b分别选自H和Me;R14为H或Me;R16a和R16b分别选自H和Me;R6选自H、OMe和OEt。
  • Aminoindane-, aminotetrahydronaphthalene- and aminobenzocyclobutane-derived PRMT5-inhibitors
    申请人:CTXT PTY LTD
    公开号:US10005792B2
    公开(公告)日:2018-06-26
    A compound of formula (1a), (1b) or (1c) wherein: n is 1 or 2; RN is H or Me; R1 is optionally one or more halo or methyl groups; R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2c and R2d (if present) are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R3a and R3b are independently selected from H and Me; R4a is selected from OH, —NH2, —C(═O)NH2, and —CH2OH; R4b is either H or Me; R5 is either H or Me; A is either (i) optionally substituted phenyl; (ii) optionally substituted naphthyl; or (iii) optionally substituted C5-12 heteroaryl.
    式(1a)、(1b)或(1c)化合物 其中:n 为 1 或 2;RN 为 H 或 Me;R1 可任选为一个或多个卤代或甲基;R2a 和 R2b 独立选自以下组:(i) F;(ii) H;(iii) Me;和 (iv) CH2OH;R2c 和 R2d(如存在)独立选自以下组:(i) F;(ii) H;(iii) Me;和 (iv) CH2OH;R3a 和 R3b 独立选自 H 和 Me;R4a 选自 OH、-NHH 或 Me:(R3a和R3b独立选自H和Me;R4a选自OH、-NH2、-C(═O)NH2和-CH2OH;R4b不是H就是Me;R5不是H就是Me;A是(i)任选取代的苯基;(ii)任选取代的萘基;或(iii)任选取代的C5-12杂芳基。
  • Tetrahydroisoquinolines as PRMT5 inhibitors
    申请人:CTXT PTY LTD
    公开号:US10421743B2
    公开(公告)日:2019-09-24
    A compound of formula (I) wherein: n is 1 or 2; p is 0 or 1; R1a, R1b, R1c and R1d are independently selected from the group consisting of H, halo, C1-4 alkoxy, C1-4 alkyl, C1-4 fluoroalkyl, C3-4 cycloalkyl, NH—C1-4 alkyl and cyano; R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2c and R2d are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2e is H or Me; R3a and R3b are independently selected from H and Me; R4 is either H or Me; R5 is either H or Me; R6a and R6b are independently selected from H and Me; A is either (i) optionally substituted phenyl; (ii) optionally substituted naphthyl; or (iii) optionally substituted C5-12 heteroaryl; wherein when R2e is H, at least one of R1a, R1b, R1c and R1d is selected from C1-4 alkoxy, C2-4 alkyl, C1-4 fluoroalkyl, C3-4 cycloalkyl, NH—C1-4 alkyl and cyano.
    式(I)化合物 其中:n 为 1 或 2;p 为 0 或 1;R1a、R1b、R1c 和 R1d 独立选自由 H、卤素、C1-4 烷氧基、C1-4 烷基、C1-4 氟烷基、C3-4 环烷基、NH-C1-4 烷基和氰基组成的组;R2a 和 R2b 独立选自由 (i) F;(ii) H;(iii) Me;和 (iv) CH2OH 组成的组;R2c 和 R2d 独立选自由 (i) F;(ii) H;(iii) Me;和 (iv) CH2OH 组成的组:(i) F;(ii) H;(iii) Me;和 (iv) CH2OH; R2e 是 H 或 Me; R3a 和 R3b 独立地选自 H 和 Me; R4 是 H 或 Me; R5 是 H 或 Me; R6a 和 R6b 独立地选自 H 和 Me; A 是 (i) 任选取代的苯基;(ii) 任选取代的萘基;或 (iii) 任选取代的 C5-12 杂芳基;其中,当 R2e 为 H 时,R1a、R1b、R1c 和 R1d 中至少有一个选自 C1-4 烷氧基、C2-4 烷基、C1-4 氟烷基、C3-4 环烷基、NH-C1-4 烷基和氰基。
  • 3-oxa-8-azabicyclo[3.2.1]octane derivatives and their use in the treatment of cancer and hemoglobinopathies
    申请人:CTXT PTY LTD
    公开号:US11028101B2
    公开(公告)日:2021-06-08
    A compound of formula Ia, Ib, Ic or Id: wherein: n is 1 or 2; RN is H or Me; R1 is optionally one or more halo or methyl groups; R2a and R2b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R2c and R2d (if present) are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R3a and R3b are independently selected from H and Me; R4a is selected from OH, —NH2, —C(═O)NH2, and —CH2OH; R4b is either H or Me; R5 is either H or Me; m is 1 or 2; q is 0 or 1; R11a, R11b, R11c and R11d are independently selected from H, halo, C1-4 alkyl, C1-4 fluoroalkyl, C3-4 cycloalkyl, C1-4 alkyloxy, NH—C1-4 alkyl and cyano; R12a and R12b are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R12c and R12d are independently selected from the group consisting of: (i) F; (ii) H; (iii) Me; and (iv) CH2OH; R12e is H or Me; R13a and R13b are independently selected from H and Me; R14 is either H or Me; R16a and R16b are independently selected from H and Me; R6 is selected from H, OMe, and OEt.
    式 Ia、Ib、Ic 或 Id 的化合物: 其中:n 为 1 或 2;RN 为 H 或 Me;R1 可任选为一个或多个卤代或甲基;R2a 和 R2b 独立选自以下组:(i) F;(ii) H;(iii) Me;和 (iv) CH2OH;R2c 和 R2d(如存在)独立选自以下组(R3a 和 R3b 独立选自 H 和 Me;R4a 选自 OH、-NH2、-C(═O)NH2 和 -CH2OH;R4b 为 H 或 Me;R5 为 H 或 Me;m 为 1 或 2;q 为 0 或 1;R11a、R11b、R11c 和 R11d 独立选自 H、卤素、C1-4 烷基、C1-4 氟烷基、C3-4 环烷基、C1-4 烷氧基、NH-C1-4 烷基和氰基; R12a 和 R12b 独立选自以下组成的组:(i) F;(ii) H;(iii) Me;和 (iv) CH2OH;R12c 和 R12d 独立地选自由以下组成的组:(i) F;(ii) H;(iii) Me;和 (iv) CH2OH;R12e 是 H 或 Me;R13a 和 R13b 独立地选自 H 和 Me;R14 是 H 或 Me;R16a 和 R16b 独立地选自 H 和 Me;R6 选自 H、OMe 和 OEt。
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