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3-Chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehyde | 433212-12-5

中文名称
——
中文别名
——
英文名称
3-Chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehyde
英文别名
3-chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehyde
3-Chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehyde化学式
CAS
433212-12-5
化学式
C13H19ClO3Si
mdl
——
分子量
286.831
InChiKey
VJKXSDVFAFDTKW-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):
    3.84
  • 重原子数:
    18
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.46
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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-Chloro-4-(2-trimethylsilylethoxymethoxy)benzaldehyde间氯过氧苯甲酸 作用下, 以 二氯甲烷 为溶剂, 生成 3-Chloro-4-(2-trimethylsilylethoxymethoxy)phenol
    参考文献:
    名称:
    Cyclohexyl(alkyl)-propanolamines, preparation method and pharmaceutical compositions containing same
    摘要:
    本发明涉及以下公式(I)的化合物: 其中,A是公式(a)或(b)的基团; 其中,R表示氢或卤素原子、—S(O)z(C1-C4)烷基、—NHSO2(C1-C4)烷基、—SO2NH(C1-C4)烷基、—NHSO2苯基-(C1-C4)烷基或—NHSO2苯基,所述苯可能被卤素原子、(C1-C4)烷基或(C1-C4)氧烷基取代; R1表示氢原子或(C1-C4)烷基、—CO(C1-C4)烷基、苯基-(C1-C4)烷基或—CO苯基,所述苯也可能被卤素原子或(C1-C4)氧烷基取代; R2是氢原子或—SO2(C1-C4)烷基、—SO2苯基-(C1-C4)烷基或—SO2苯基; X完成5至8个原子的环,该环饱和或不饱和,可能被一个或两个(C1-C4)烷基取代,并带有一个或两个羰基基团; n,m和z独立地为0,1或2; R3表示氢或卤素原子、(C1-C6)烷基、(C1-C4)氧烷基、—COO(C1-C4)烷基、—CO(C1-C4)烷基、—NHSO2(C1-C4)烷基、—NHSO2苯基-(C1-C4)烷基、—NO2、—CN、—CONR4R5、—COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基; R4和R5独立地表示氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基,或R4和R5与它们所连接的氮原子可以总共形成5至7个原子的环;以及其盐或溶剂化物、含有它们的制药组合物、制备它们的过程和该过程中的中间体。
    公开号:
    US20040053916A1
  • 作为产物:
    参考文献:
    名称:
    Cyclohexyl(alkyl)-propanolamines, preparation method and pharmaceutical compositions containing same
    摘要:
    本发明涉及以下公式(I)的化合物: 其中,A是公式(a)或(b)的基团; 其中,R表示氢或卤素原子、—S(O)z(C1-C4)烷基、—NHSO2(C1-C4)烷基、—SO2NH(C1-C4)烷基、—NHSO2苯基-(C1-C4)烷基或—NHSO2苯基,所述苯可能被卤素原子、(C1-C4)烷基或(C1-C4)氧烷基取代; R1表示氢原子或(C1-C4)烷基、—CO(C1-C4)烷基、苯基-(C1-C4)烷基或—CO苯基,所述苯也可能被卤素原子或(C1-C4)氧烷基取代; R2是氢原子或—SO2(C1-C4)烷基、—SO2苯基-(C1-C4)烷基或—SO2苯基; X完成5至8个原子的环,该环饱和或不饱和,可能被一个或两个(C1-C4)烷基取代,并带有一个或两个羰基基团; n,m和z独立地为0,1或2; R3表示氢或卤素原子、(C1-C6)烷基、(C1-C4)氧烷基、—COO(C1-C4)烷基、—CO(C1-C4)烷基、—NHSO2(C1-C4)烷基、—NHSO2苯基-(C1-C4)烷基、—NO2、—CN、—CONR4R5、—COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基; R4和R5独立地表示氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基,或R4和R5与它们所连接的氮原子可以总共形成5至7个原子的环;以及其盐或溶剂化物、含有它们的制药组合物、制备它们的过程和该过程中的中间体。
    公开号:
    US20040053916A1
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文献信息

  • CYCLOHEXYL(ALKYL)PROPANOLAMINES, PREPARATION METHOD AND PHARMACEUTICAL COMPOSITIONS CONTAINING SAME
    申请人:Bovy Philippe R.
    公开号:US20080261949A1
    公开(公告)日:2008-10-23
    The present invention relates to the compounds of formula (I): in which A is a group of formula (a) or (b) in which R represents a hydrogen or halogen atom, an —S(O) z (C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —SO 2 NH(C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl group or an —NHSO 2 phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C 1 -C 4 )alkyl group or with a (C 1 -C 4 )alkoxy group; R 1 represents a hydrogen atom or a (C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, a phenyl-(C 1 -C 4 )alkyl group or a —COphenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C 1 -C 4 )alkoxy group; R 2 is a hydrogen atom or an —SO 2 (C 1 -C 4 )alkyl group, an —SO 2 phenyl-(C 1 -C 4 )alkyl group or an —SO 2 phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C 1 -C 4 )alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R 3 represents a hydrogen or halogen atom, a (C 1 -C 6 )alkyl group, a (C 1 -C 4 )alkoxy group, a —COO(C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl groups, —NO 2 , —CN, —CONR 4 R 5 , —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R 4 and R 5 represent, independently, a hydrogen atom, a phenyl, a (C 1 -C 4 )alkyl group or a phenyl-(C 1 -C 4 )alkyl group or R 4 and R 5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.
    本发明涉及公式(I)的化合物: 其中A是公式(a)或(b)的基团: 其中R表示氢或卤素原子,-S(O)z(C1-C4)烷基,-NHSO2(C1-C4)烷基,-SO2NH(C1-C4)烷基,-NHSO2苯基-(C1-C4)烷基或-NHSO2苯基,所述苯基可能被卤素原子,(C1-C4)烷基或(C1-C4)氧烷基取代; R1表示氢原子或(C1-C4)烷基,-CO(C1-C4)烷基,苯基-(C1-C4)烷基或-CO苯基,所述苯基也可能被卤素原子或(C1-C4)氧烷基取代; R2是氢原子或-SO2(C1-C4)烷基,-SO2苯基-(C1-C4)烷基或-SO2苯基; X完成由5到8个原子组成的环,该环饱和或不饱和,可能被一个或两个(C1-C4)烷基取代,并带有一个或两个羰基基团; n,m和z独立地为0、1或2; R3表示氢或卤素原子,(C1-C6)烷基,(C1-C4)氧烷基,-COO(C1-C4)烷基,-CO(C1-C4)烷基,-NHSO2(C1-C4)烷基,-NHSO2苯基-(C1-C4)烷基,-NO2,-CN,-CONR4R5,-COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基; R4和R5独立地表示氢原子,苯基,(C1-C4)烷基或苯基-(C1-C4)烷基,或R4和R5与它们附着的氮原子一起可以形成总共5到7个原子的环;以及其盐或溶剂,含有它们的制药组合物,制备过程和其中间体的本发明。
  • Cyclohexyl(alkyl)propanolamines, Preparation Method and Pharmaceutical Compositions Containing Same
    申请人:BOVY R. Philippe
    公开号:US20070015745A1
    公开(公告)日:2007-01-18
    The present invention relates to the compounds of formula (I): in which A is a group of formula (a) or (b) in which R represents a hydrogen or halogen atom, an —S(O) z (C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —SO 2 NH(C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl group or an —NHSO 2 phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C 1 -C 4 )alkyl group or with a (C 1 -C 4 )alkoxy group; R 1 represents a hydrogen atom or a (C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, a phenyl-(C 1 -C 4 )alkyl group or a —CO—phenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C 1 -C 4 )alkoxy group; R 2 is a hydrogen atom or an —SO 2 (C 1 -C 4 )alkyl group, an —SO 2 phenyl-(C 1 -C 4 )alkyl group or an —SO 2 phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C 1 -C 4 )alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R 3 represents a hydrogen or halogen atom, a (C 1 -C 6 )alkyl group, a (C 1 -C 4 )alkoxy group, a —COO(C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl groups, —NO 2 , —CN, —CONR 4 R 5 , —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R4 and R 5 represent, independently, a hydrogen atom, a phenyl, a (C 1 -C 4 )alkyl group or a phenyl-(C 1 -C 4 )alkyl group or R 4 and R 5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.
    本发明涉及式(I)的化合物: 其中,A是式(a)或(b)的基团: 其中,R代表氢或卤素原子,-S(O)z(C1-C4)烷基,-NHSO2(C1-C4)烷基,-SO2NH(C1-C4)烷基,-NHSO2苯基-(C1-C4)烷基或-NHSO2苯基,所述苯可能被卤素原子,(C1-C4)烷基或(C1-C4)氧代基取代;R1代表氢原子或(C1-C4)烷基,-CO(C1-C4)烷基,苯基-(C1-C4)烷基或-CO-苯基,所述苯也可能被卤素原子或(C1-C4)氧代基取代;R2是氢原子或-SO2(C1-C4)烷基,-SO2苯基-(C1-C4)烷基或-SO2苯基;X完成一个由5到8个原子组成的环,该环饱和或不饱和,可能被一个或两个(C1-C4)烷基取代,并带有一个或两个羰基基团;n,m和z独立地为0,1或2;R3代表氢或卤素原子,(C1-C6)烷基,(C1-C4)氧代基,-COO(C1-C4)烷基,-CO(C1-C4)烷基,-NHSO2(C1-C4)烷基,-NHSO2苯基-(C1-C4)烷基,-NO2,-CN,-CONR4R5,-COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基;R4和R5独立地代表氢原子,苯基,(C1-C4)烷基或苯基-(C1-C4)烷基,或R4和R5与它们所连接的氮原子可以总共形成一个由5到7个原子组成的环;以及它们的盐或溶剂合物,含有它们的制药组合物,制备它们的过程以及在该过程中的中间体。
  • Cyclohexyl(alkyl)propanolamines, preparation method and pharmaceutical compositions containing same
    申请人:Sanofi-Aventis
    公开号:US07419974B2
    公开(公告)日:2008-09-02
    The present invention relates to the compounds of formula (I): in which A is a group of formula (a) or (b) in which R represents a hydrogen or halogen atom, an —S(O)z(C1-C4)alkyl group, an —NHSO2(C1-C4)alkyl group, an —SO2NH(C1-C4)alkyl group, an —NHSO2phenyl-(C1-C4)alkyl group or an —NHSO2phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C1-C4)alkyl group or with a (C1-C4)alkoxy group; R1 represents a hydrogen atom or a (C1-C4)alkyl group, a —CO(C1-C4)alkyl group, a phenyl-(C1-C4)alkyl group or a —COphenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C1-C4)alkoxy group; R2 is a hydrogen atom or an —SO2(C1-C4)alkyl group, an —SO2phenyl-(C1-C4)alkyl group or an —SO2phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C1-C4)alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R3 represents a hydrogen or halogen atom, a (C1-C6)alkyl group, a (C1-C4)alkoxy group, a —COO(C1-C4)alkyl group, a —CO(C1-C4)alkyl group, an —NHSO2(C1-C4)alkyl group, an —NHSO2phenyl-(C1-C4)alkyl groups, —NO2, —CN, —CONR4R5, —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R4 and R5 represent, independently, a hydrogen atom, a phenyl, a (C1-C4)alkyl group or a phenyl-(C1-C4)alkyl group or R4 and R5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.
    本发明涉及式(I)的化合物: 其中,A是式(a)或(b)的基团,其中R代表氢原子或卤素原子,-S(O)z(C1-C4)烷基,-NHSO2(C1-C4)烷基,-SO2NH(C1-C4)烷基,-NHSO2苯基-(C1-C4)烷基或-NHSO2苯基,所述苯基可能被卤素原子、(C1-C4)烷基或(C1-C4)烷氧基取代;R1代表氢原子或(C1-C4)烷基,-CO(C1-C4)烷基,苯基-(C1-C4)烷基或-CO苯基,所述苯基也可能被卤素原子或(C1-C4)烷氧基取代;R2是氢原子或-SO2(C1-C4)烷基,-SO2苯基-(C1-C4)烷基或-SO2苯基;X完成5到8个原子的环,该环饱和或不饱和,可能被一个或两个(C1-C4)烷基取代,且带有一个或两个羰基;n、m和z分别为0、1或2;R3代表氢原子或卤素原子、(C1-C6)烷基、(C1-C4)烷氧基、-COO(C1-C4)烷基、-CO(C1-C4)烷基、-NHSO2(C1-C4)烷基、-NHSO2苯基-(C1-C4)烷基、-NO2、-CN、-CONR4R5、-COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基;R4和R5分别代表氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基,或R4和R5与它们所连接的氮原子一起可以形成总共5到7个原子的环;以及其盐或溶剂,以及包含它们的制药组合物、制备它们的过程和该过程中的中间体。
  • Cyclohexyl(alkyl)-propanolamines, preparation method and pharmaceutical compositions containing same
    申请人:——
    公开号:US20040053916A1
    公开(公告)日:2004-03-18
    The present invention relates to the compounds of formula (I): 1 in which A is a group of formula (a) or (b) 2 in which R represents a hydrogen or halogen atom, an —S(O) z (C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —SO 2 NH(C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl group or an —NHSO 2 phenyl group, said phenyl possibly being substituted with a halogen atom, with a (C 1 -C 4 )alkyl group or with a (C 1 -C 4 )alkoxy group; R 1 represents a hydrogen atom or a (C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, a phenyl-(C 1 -C 4 )alkyl group or a —COphenyl group, said phenyl also possibly being substituted with a halogen atom or with a (C 1 -C 4 )alkoxy group; R 2 is a hydrogen atom or an —SO 2 (C 1 -C 4 )alkyl group, an —SO 2 phenyl-(C 1 -C 4 )alkyl group or an —SO 2 phenyl group; X completes a ring of 5 to 8 atoms, said ring being saturated or unsaturated, possibly being substituted with one or two (C 1 -C 4 )alkyl groups and bearing one or two carbonyl groups; n, m and z are, independently, 0, 1 or 2; R 3 represents a hydrogen or halogen atom, a (C 1 -C 6 )alkyl group, a (C 1 -C 4 )alkoxy group, a —COO(C 1 -C 4 )alkyl group, a —CO(C 1 -C 4 )alkyl group, an —NHSO 2 (C 1 -C 4 )alkyl group, an —NHSO 2 phenyl-(C 1 -C 4 )alkyl groups, —NO 2 , —CN, —CONR 4 R 5 , —COOH, or a 4,5-dihydro-1,3-oxazol-2-yl or 4,4-dimethyl-4,5-dihydro-1,3-oxazol-2-yl group; R 4 and R 5 represent, independently, a hydrogen atom, a phenyl, a (C 1 -C 4 )alkyl group or a phenyl-(C 1 -C 4 )alkyl group or R 4 and R 5 with the nitrogen atom to which they are attached, may form a ring of 5 to 7 atoms in total; and to the salts or solvates thereof, to the pharmaceutical compositions containing them, to a process for the preparation thereof and to intermediates in this process.
    本发明涉及以下公式(I)的化合物: 其中,A是公式(a)或(b)的基团; 其中,R表示氢或卤素原子、—S(O)z(C1-C4)烷基、—NHSO2(C1-C4)烷基、—SO2NH(C1-C4)烷基、—NHSO2苯基-(C1-C4)烷基或—NHSO2苯基,所述苯可能被卤素原子、(C1-C4)烷基或(C1-C4)氧烷基取代; R1表示氢原子或(C1-C4)烷基、—CO(C1-C4)烷基、苯基-(C1-C4)烷基或—CO苯基,所述苯也可能被卤素原子或(C1-C4)氧烷基取代; R2是氢原子或—SO2(C1-C4)烷基、—SO2苯基-(C1-C4)烷基或—SO2苯基; X完成5至8个原子的环,该环饱和或不饱和,可能被一个或两个(C1-C4)烷基取代,并带有一个或两个羰基基团; n,m和z独立地为0,1或2; R3表示氢或卤素原子、(C1-C6)烷基、(C1-C4)氧烷基、—COO(C1-C4)烷基、—CO(C1-C4)烷基、—NHSO2(C1-C4)烷基、—NHSO2苯基-(C1-C4)烷基、—NO2、—CN、—CONR4R5、—COOH或4,5-二氢-1,3-噁唑-2-基或4,4-二甲基-4,5-二氢-1,3-噁唑-2-基; R4和R5独立地表示氢原子、苯基、(C1-C4)烷基或苯基-(C1-C4)烷基,或R4和R5与它们所连接的氮原子可以总共形成5至7个原子的环;以及其盐或溶剂化物、含有它们的制药组合物、制备它们的过程和该过程中的中间体。
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