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4-Methoxy-3-(4-phenyl-piperazine-1-sulfonyl)-benzoic acid

中文名称
——
中文别名
——
英文名称
4-Methoxy-3-(4-phenyl-piperazine-1-sulfonyl)-benzoic acid
英文别名
4-methoxy-3-(4-phenylpiperazin-1-yl)sulfonylbenzoic acid
4-Methoxy-3-(4-phenyl-piperazine-1-sulfonyl)-benzoic acid化学式
CAS
——
化学式
C18H20N2O5S
mdl
——
分子量
376.4
InChiKey
NQHOHXVXCHLYFB-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):
    2.2
  • 重原子数:
    26
  • 可旋转键数:
    5
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    95.5
  • 氢给体数:
    1
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Aryl sulfonic acids and derivatives as FSH antagonists
    摘要:
    本发明提供了式I的化合物,其具有结构1, 其中, Q为氢或—SO2R1; X为键合,O,S(O)n,—CH═CH—,—CH2CH2—,—C≡C—或—CH2S(O)nCH2—; R1为OH,NH2,C1到C6烷氧基,C1到C3全氟烷氧基; R2和R4各自独立地为氢,OR6,—S(O)mR6,—NHR6,—N(R6)2或—CH2SO2CH3; R3和R5各自独立地为氢,—NO2,—NH2,—SO2R9或—CH2R9; R6为氢,C1到C6烷基,C3到C6烯基,—CH2CH2Z,—CH2COR7,—CH2CH═CHCOR73; Y1和Y3各自独立地为N或CH; Y2和Y4各自独立地为O,S或NR13; R7为—OR8,—NHR8,—N(R8)2或—NHCH2CH2OR8; Z为—OR8,—OCH2CH2OR8,—N(R8)2或 4 R8为氢或C1到C3烷基; R9为C1到C6烷基,C3到C6烯基,OH,NHR10,N(R10)2,CH2COR11,—CH2CH═CHCOR11或 5 R10为C1到C3烷基,C3到C4烯基,苯基,—CH2CH2OCH3或 6 R11为—OR12,NHR12,—N(R12)2或—NHCH2CH2OR12; R12为氢或C1到C3烷基; R13为氢或C1到C3烷基; W为键合,CH2,CH2CH2,O,S(O)q,NCHO,NCOCH3或NR12; m为0-2; n为0-2; q为0-2; 但R2和R3不能同时为氢; 或其药学上可接受的盐,其作为避孕剂具有用途。
    公开号:
    US20020111369A1
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文献信息

  • [EN] ARYL SULFONIC ACIDS AND DERIVATIVES AS FSH ANTAGONISTS<br/>[FR] ACIDES SULFONIQUES ARYLES ET DERIVES TELS QUE LES ANTAGONISTES FSH
    申请人:AMERICAN HOME PROD
    公开号:WO2000058277A1
    公开(公告)日:2000-10-05
    This invention provides compounds of formula (I) having the structure wherein Q is hydrogen or -SO2R1; X is a bond, O, S(O)¿n?, -CH=CH-, -CH2CH2-, -C C-, or -CH2S(O)nCH2-; R?1¿ is OH, NH¿2?, C1 to C6 alkoxy, C1 to C3 perfluoroalkoxy; Ar is (a) or (b); Ar' is (c) or (d); R?2 and R4¿ are each, independently, hydrogen, OR6, -S(O)¿m?R?6, -NHR6, -N(R6)¿2, or -CH2SO2CH3; R?3 and R5¿ are each, independently, hydrogen, -NO¿2?, -NH2, -SO2R?9¿, or -CH¿2R?9; R6 is hydrogen, C¿1? to C6 alkyl, C3 to C6 alkenyl, -CH2CH2Z, -CH2COR?7, -CH¿2CH=CHCOR7, (e), (f) or (g); Y¿1? and Y?3¿ are each, independently, N, or CH; Y?2 and Y4¿ are each independently, O, S, or NR?13; R7 is -OR8, -NHR8, -N(R8)¿2, or -NHCH2CH2OR8; Z is -OR¿8?, -OCH2CH2OR?8, -N(R8)¿2, or (h); R8 is hydrogen or C1 to C3 alkyl; R9 is C1 to C6 alkyl, C3 to C6 alkenyl, OH, NHR?10, N(R10)¿2, CH2COR11, -CH2CH=CHCOR11, or (i); R10 is C1 to C3 alkyl, C3 to C4 alkenyl, phenyl, -CH2CH2OCH3, or -(j); R?11 is -OR12, -NHR12, -N(R12)¿2, or -NHCH2CH2OR12; R12 is hydrogen, or C¿1? to C3 alkyl; R?13¿ is hydrogen, or C¿1? to C3 alkyl; W is a bond, CH2, CH2CH2, O, S(O)q, NCHO, NCOCH3, or NR?12¿; m is 0 - 2; n is 0 - 2; q is 0 - 2, with the proviso that R?2 and R3¿ are not both hydrogen; or pharmaceutically acceptable salt thereof, which are useful as contraceptive agents.
    本发明提供了具有结构式(I)的化合物,其中Q为氢或-SO2R1; X为键,O,S(O)n,-CH=CH-,- -,-CC-或-CH2S(O)n -; R1为OH,NH2,C1到C6烷氧基,C1到C3全氟烷氧基; Ar为(a)或(b); Ar'为(c)或(d); R2和R4分别独立地为氢,OR6,-S(O)mR6,-NHR6,-N(R6)2或- O2CH3; R3和R5独立地为氢,-NO2,-NH2,-SO2R9或- R9; R6为氢,C1到C6烷基,C3到C6烯基,- Z,- COR7,- CH=CHCOR7,(e),(f)或(g); Y1和Y3独立地为N或CH; Y2和Y4独立地为O,S或NR13; R7为-OR8,-NHR8,-N(R8)2或-NH OR8; Z为-OR8,-O OR8,-N(R8)2或(h); R8为氢或C1到C3烷基; R9为C1到C6烷基,C3到C6烯基,OH,NHR10,N(R10)2, COR11,- CH=CHCOR11或(i); R10为C1到C3烷基,C3到C4烯基,苯基,- OCH3或-(j); R11为-OR12,-NHR12,-N(R12)2或-NH OR12; R12为氢或C1到C3烷基; R13为氢或C1到C3烷基; W为键,CH2, ,O,S(O)q,NCHO,NCOCH3或NR12; m为0-2; n为0-2; q为0-2,但R2和R3不能同时为氢; 或其药学上可接受的盐,其作为避孕剂有用。
  • US6355633B1
    申请人:——
    公开号:US6355633B1
    公开(公告)日:2002-03-12
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