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5-amino-1-(1-methyl-2-oxo-2-phenyl-ethyl)-1H-pyrazole-4-carboxylic acid ethyl ester

中文名称
——
中文别名
——
英文名称
5-amino-1-(1-methyl-2-oxo-2-phenyl-ethyl)-1H-pyrazole-4-carboxylic acid ethyl ester
英文别名
ethyl 5-amino-1-(1-oxo-1-phenylpropan-2-yl)pyrazole-4-carboxylate
5-amino-1-(1-methyl-2-oxo-2-phenyl-ethyl)-1H-pyrazole-4-carboxylic acid ethyl ester化学式
CAS
——
化学式
C15H17N3O3
mdl
——
分子量
287.318
InChiKey
QMXFMVGQPJPFTC-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):
    2.6
  • 重原子数:
    21
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    87.2
  • 氢给体数:
    1
  • 氢受体数:
    5

反应信息

  • 作为反应物:
    描述:
    5-amino-1-(1-methyl-2-oxo-2-phenyl-ethyl)-1H-pyrazole-4-carboxylic acid ethyl ester 在 sodium tetrahydroborate 作用下, 以 乙醇 为溶剂, 反应 0.5h, 以98%的产率得到5-amino-1-(2-hydroxy-1-methyl-2-phenylethyl)-1H-pyrazole-4-carboxylic acid ethyl ester
    参考文献:
    名称:
    Substituted pyrazolo[1,5-A] pyrimidines as calcium receptor modulating agents
    摘要:
    提供了一种包括式(I)化合物的钙受体调节剂: 其中环A是可选择地取代的5-至7-成员环;环B是可选择地取代的5-至7-成员杂环;X1是CR1、CR1R2、N或NR13;X2是N或NR3;Y是C、CR4或N,Z是CR5、CR5R6、N或NR7;Ar是可选择地取代的环状基团;R是H、可选择地取代的碳氢基团等;和是单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H、可选择地取代的碳氢基团;或其盐或前药。还提供了式(II)和(III)的化合物: 其中环A是可选择地取代的5-至7-成员环;Q是C、CR5或N;R8、R9、R10、R11和R12独立地是H、可选择地取代的碳氢基团等,或其盐。 还请在式(II)和(III)中指定X1、R3、R1、Y和X3。
    公开号:
    US09447100B2
  • 作为产物:
    描述:
    3-氨基-4-乙氧羰基吡唑2-溴苯丙酮 在 sodium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 48.0h, 以12%的产率得到5-amino-1-(1-methyl-2-oxo-2-phenyl-ethyl)-1H-pyrazole-4-carboxylic acid ethyl ester
    参考文献:
    名称:
    Substituted pyrazolo[1,5-A] pyrimidines as calcium receptor modulating agents
    摘要:
    提供了一种包括式(I)化合物的钙受体调节剂: 其中环A是可选择地取代的5-至7-成员环;环B是可选择地取代的5-至7-成员杂环;X1是CR1、CR1R2、N或NR13;X2是N或NR3;Y是C、CR4或N,Z是CR5、CR5R6、N或NR7;Ar是可选择地取代的环状基团;R是H、可选择地取代的碳氢基团等;和是单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H、可选择地取代的碳氢基团;或其盐或前药。还提供了式(II)和(III)的化合物: 其中环A是可选择地取代的5-至7-成员环;Q是C、CR5或N;R8、R9、R10、R11和R12独立地是H、可选择地取代的碳氢基团等,或其盐。 还请在式(II)和(III)中指定X1、R3、R1、Y和X3。
    公开号:
    US09447100B2
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文献信息

  • Calcium receptor modulating compound and use thereof
    申请人:Yasuma Tsuneo
    公开号:US20060079536A1
    公开(公告)日:2006-04-13
    There is provided a calcium receptor modulator comprising a compound of the formula (I): wherein ring A is an optionally substituted 5- to 7-membered ring; ring B is an optionally substituted 5- to 7-membered heterocyclic ring; X 1 is CR 1 , CR 1 R 2 , N or NR 13 ; X 2 is N or NR 3 ; Y is C, CR 4 or N, Z is CR 5 , CR 5 R 6 , N or NR 7 ; Ar is an optionally substituted cyclic group; R is H, an optionally substituted hydrocarbon group, etc.; and is a single bond or a double bond; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 13 are independently H, an optionally substituted hydrocarbon group; or a salt thereof or a prodrug thereof. Compounds of the formula (II) and (III): wherein ring A is an optionally substituted 5- to 7-membered ring; Q is C, CR 5 or N; R 8 , R 9 , R 10 , R 11 and R 12 are independently, H, an optionally substituted hydrocarbon group, etc., or a salt thereof are also provided. Also specify X 1 , R 3 , R 1 , Y and X 3 in formula (II) and (III) as before.
    提供了一种含有式(I)化合物的钙受体调节剂:其中,环A是可选取代的5-至7-成员环;环B是可选取代的5-至7-成员杂环;X1是CR1、CR1R2、N或NR13;X2是N或NR3;Y是C、CR4或N;Z是CR5、CR5R6、N或NR7;Ar是可选取代的环状基团;R是H、可选取代的碳氢基团等;是单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H、可选取代的碳氢基团;或其盐或前药。还提供了式(II)和(III)化合物:其中,环A是可选取代的5-至7-成员环;Q是C、CR5或N;R8、R9、R10、R11和R12独立地是H、可选取代的碳氢基团等;或其盐。在式(II)和(III)中,X1、R3、R1、Y和X3的指定与之前相同。
  • Substituted pyrazolo [1,5-A]pyrimidines as calcium receptor modulating agents
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US07514441B2
    公开(公告)日:2009-04-07
    There is provided a calcium receptor modulator comprising a compound of the formula (I): wherein ring A is an optionally substituted 5- to 7-membered ring; ring B is an optionally substituted 5- to 7-membered heterocyclic ring; X1 is CR1, CR1R2, N or NR13; X2 is N or NR3; Y is C, CR4 or N, Z is CR5, CR5R6, N or NR7; Ar is an optionally substituted cyclic group; R is H, an optionally substituted hydrocarbon group, etc.; and  is a single bond or a double bond; R1, R2, R3, R4, R5, R6, R7 and R13 are independently H, an optionally substituted hydrocarbon group; or a salt thereof or a prodrug thereof. Compounds of the formula (II) and (III): wherein ring A is an optionally substituted 5- to 7-membered ring; Q is C, CR5 or N; R8, R9, R10, R11 and R12 are independently, H, an optionally substituted hydrocarbon group, etc., or a salt thereof are also provided. Also specify X1, R3, R1, Y and X3 in formula (II) and (III) as before.
    提供了一种钙受体调节剂,包括式(I)的化合物:其中环A是可选取代的5-至7成员环;环B是可选取代的5-至7成员杂环;X1是CR1,CR1R2,N或NR13;X2是N或NR3;Y是C,CR4或N,Z是CR5,CR5R6,N或NR7;Ar是可选取代的环状基团;R是H,可选取代的烃基团等; 是单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H,可选取代的烃基团;或其盐或前药。还提供了式(II)和(III)的化合物:其中环A是可选取代的5-至7成员环;Q是C,CR5或N;R8、R9、R10、R11和R12独立地是H,可选取代的烃基团等,或其盐。同样在式(II)和(III)中指定X1、R3、R1、Y和X3,如前所述。
  • SUBSTITUTED PYRAZOLO[1,5-A] PYRIMIDINES AS CALCIUM RECEPTOR MODULATING AGENTS
    申请人:Takeda Pharmaceutical Company Limited
    公开号:US20140155416A1
    公开(公告)日:2014-06-05
    There is provided a calcium receptor modulator comprising a compound of the formula (I): wherein ring A is an optionally substituted 5- to 7-membered ring; ring B is an optionally substituted 5- to 7-membered heterocyclic ring; X 1 is CR 1 , CR 1 R 2 , N or NR 13 ; X 2 is N or NR 3 ; Y is C, CR 4 or N, Z is CR 5 , CR 5 R 6 , N or NR 7 ; Ar is an optionally substituted cyclic group; R is H, an optionally substituted hydrocarbon group, etc.; and is a single bond or a double bond; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 13 are independently H, an optionally substituted hydrocarbon group; or a salt thereof or a prodrug thereof. Compounds of the formula (II) and (III): wherein ring A is an optionally substituted 5- to 7-membered ring; Q is C, CR 5 or N; R 8 , R 9 , R 10 , R 11 and R 12 are independently, H, an optionally substituted hydrocarbon group, etc., or a salt thereof are also provided. Also specify X 1 , R 3 , R 1 , Y and X 3 in formula (II) and (III) as before.
    提供了一种含有式(I)化合物的钙受体调节剂,其中环A是可选取代的5-至7元环;环B是可选取代的5-至7元杂环;X1是CR1,CR1R2,N或NR13;X2是N或NR3;Y是C,CR4或N,Z是CR5,CR5R6,N或NR7;Ar是可选取代的环状基团;R是H,可选取代的烃基团等;表示单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H,可选取代的烃基团;或其盐或前药。还提供了式(II)和(III)的化合物:其中环A是可选取代的5-至7元环;Q是C,CR5或N;R8、R9、R10、R11和R12独立地是H,可选取代的烃基团等,或其盐。同样指定式(II)和(III)中的X1、R3、R1、Y和X3如前。
  • SUBSTITUTED PYRAZOLO[1,5-A]PYRIMIDINES AS CALCIUM RECEPTOR MODULATING AGENTS
    申请人:Yasuma Tsuneo
    公开号:US20090215746A1
    公开(公告)日:2009-08-27
    There is provided a calcium receptor modulator comprising a compound of the formula (I): wherein ring A is an optionally substituted 5- to 7-membered ring; ring B is an optionally substituted 5- to 7-membered heterocyclic ring; X 1 is CR 1 , CR 1 R 2 , N or NR 13 ; X 2 is N or NR 3 ; Y is C, CR 4 or N, Z is CR 5 , CR 5 R 6 , N or NR 7 ; Ar is an optionally substituted cyclic group; R is H, an optionally substituted hydrocarbon group, etc.; and is a single bond or a double bond; R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , R 7 and R 13 are independently H, an optionally substituted hydrocarbon group; or a salt thereof or a prodrug thereof. Compounds of the formula (II) and (III): wherein ring A is an optionally substituted 5- to 7-membered ring; Q is C, CR 5 or N; R 8 , R 9 , R 10 , R 11 and R 12 are independently, H, an optionally substituted hydrocarbon group, etc., or a salt thereof are also provided. Also specify X 1 , R 3 , R 1 , Y and X 3 in formula (II) and (III) as before.
    提供了一种包含式(I)化合物的钙受体调节剂,其中环A是可选取代的5-至7-成员环;环B是可选取代的5-至7-成员杂环;X1是CR1、CR1R2、N或NR13;X2是N或NR3;Y是C、CR4或N,Z是CR5、CR5R6、N或NR7;Ar是可选取代的环状基团;R是H、可选取代的碳氢基团等;和是单键或双键;R1、R2、R3、R4、R5、R6、R7和R13独立地是H、可选取代的碳氢基团;或其盐或前药。还提供了式(II)和(III)化合物:其中环A是可选取代的5-至7-成员环;Q是C、CR5或N;R8、R9、R10、R11和R12独立地是H、可选取代的碳氢基团等,或其盐。同时,如前所述,还指定式(II)和(III)中的X1、R3、R1、Y和X3。
  • CALCIUM RECEPTOR MODULATING COMPOUND AND USE THEREOF
    申请人:Takeda Pharmaceutical Company Limited
    公开号:EP1572113B1
    公开(公告)日:2017-05-17
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