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dl-1-benzyl-5-benzyloxy-2-methyl-7-(5-phenyl-2-pentyloxy)-4-oxo-1,2,3,4-tetrahydroquinoline | 98834-55-0

中文名称
——
中文别名
——
英文名称
dl-1-benzyl-5-benzyloxy-2-methyl-7-(5-phenyl-2-pentyloxy)-4-oxo-1,2,3,4-tetrahydroquinoline
英文别名
1-Benzyl-5-benzyloxy-2-methyl-7-(5-phenyl-2-pentyloxy)-4-oxo-1,2,3,4-tetrahydroquinoline;1-benzyl-2-methyl-5-phenylmethoxy-7-(5-phenylpentan-2-yloxy)-2,3-dihydroquinolin-4-one
dl-1-benzyl-5-benzyloxy-2-methyl-7-(5-phenyl-2-pentyloxy)-4-oxo-1,2,3,4-tetrahydroquinoline化学式
CAS
98834-55-0
化学式
C35H37NO3
mdl
——
分子量
519.684
InChiKey
DGVKPWYKYVVNFU-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):
    8
  • 重原子数:
    39
  • 可旋转键数:
    11
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    38.8
  • 氢给体数:
    0
  • 氢受体数:
    4

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
  • 下游产品
    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:
    参考文献:
    名称:
    Bicyclic benzo fused compounds
    摘要:
    公式为##STR1##的双环融合苯类化合物及其药学上可接受的阳离子和酸盐,其中M为O、CH.sub.2或NR.sub.6;R.sub.6为氢、甲酰基、羟甲基苄氧基或某些羧烷氧基烷基、烷酰基、烷基、芳基烷基或芳基烷基羰基基团;A'为:(1) A,其中A和B中的一个为氢,使得当A为氢时,B为C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q且f为1或2;当B为氢时,A为C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q且f为0或1,当A和OR.sub.1一起形成内酯或其某些衍生物时;(2) A'为##STR2##(3) A'为Q.sub.3;Q为CO.sub.2 R.sub.7、COR.sub.8、C(OH)R.sub.8 R.sub.9、CN、CONR.sub.12 R.sub.13、CH.sub.2 NR.sub.12 R.sub.13、CH.sub.2 NHCOR.sub.14、CH.sub.2 NHSO.sub.2 R.sub.17或5-四唑基;Q.sub.3为##STR3##5-四唑基、CH.sub.2 CONHCOR.sub.7、COOH或其某些酯、酰胺、羧酰亚胺或磺酰亚胺衍生物,CONHOH、CONHCONH.sub.2或COCH.sub.2 Q.sub.4,其中Q.sub.4为CN或COOH或其某些酯;R.sub.1为氢、苄基或某些酰基;R.sub.4为氢、某些烷基或某些芳基烷基;R.sub.5为氢或某些烷基;Z为(C.sub.1-C.sub.9)烷基,可由O、S、SO或SO.sub.2中断;W为氢、甲基、某些芳基或环烷基;在哺乳动物中作为镇痛剂、镇静剂、止吐剂、利尿剂、抗癫痫药、止泻药、镇咳剂、治疗青光眼和其中间体。
    公开号:
    US04486428A1
  • 作为产物:
    参考文献:
    名称:
    Bicyclic benzo fused compounds
    摘要:
    公式为##STR1##的双环融合苯类化合物及其药学上可接受的阳离子和酸盐,其中M为O、CH.sub.2或NR.sub.6;R.sub.6为氢、甲酰基、羟甲基苄氧基或某些羧烷氧基烷基、烷酰基、烷基、芳基烷基或芳基烷基羰基基团;A'为:(1) A,其中A和B中的一个为氢,使得当A为氢时,B为C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q且f为1或2;当B为氢时,A为C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q且f为0或1,当A和OR.sub.1一起形成内酯或其某些衍生物时;(2) A'为##STR2##(3) A'为Q.sub.3;Q为CO.sub.2 R.sub.7、COR.sub.8、C(OH)R.sub.8 R.sub.9、CN、CONR.sub.12 R.sub.13、CH.sub.2 NR.sub.12 R.sub.13、CH.sub.2 NHCOR.sub.14、CH.sub.2 NHSO.sub.2 R.sub.17或5-四唑基;Q.sub.3为##STR3##5-四唑基、CH.sub.2 CONHCOR.sub.7、COOH或其某些酯、酰胺、羧酰亚胺或磺酰亚胺衍生物,CONHOH、CONHCONH.sub.2或COCH.sub.2 Q.sub.4,其中Q.sub.4为CN或COOH或其某些酯;R.sub.1为氢、苄基或某些酰基;R.sub.4为氢、某些烷基或某些芳基烷基;R.sub.5为氢或某些烷基;Z为(C.sub.1-C.sub.9)烷基,可由O、S、SO或SO.sub.2中断;W为氢、甲基、某些芳基或环烷基;在哺乳动物中作为镇痛剂、镇静剂、止吐剂、利尿剂、抗癫痫药、止泻药、镇咳剂、治疗青光眼和其中间体。
    公开号:
    US04486428A1
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文献信息

  • Benzopyrans
    申请人:Pfizer Inc.
    公开号:US04680404A1
    公开(公告)日:1987-07-14
    Bicyclic fused benzenoid compounds of the formula ##STR1## and pharmaceutically acceptable cationic and acid addition salts thereof, where M is O, CH.sub.2 or NR.sub.6 ; R.sub.6 is hydrogen, formyl, carbobenzyloxy or certain carboalkoxyalkyl, alkanoyl, alkyl, aralkyl or aralkylcarbonyl groups; A' is: (1) A where one of A and B is hydrogen such that when A is hydrogen, B is C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q and f is 1 or 2; when B is hydrogen, A is C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q and f is 0 or 1, when taken together A and OR.sub.1 form a lactone or certain derivatives thereof; (2) A' is ##STR2## (3) A' is Q.sub.3 ; Q is CO.sub.2 R.sub.7, COR.sub.8, C(OH)R.sub.8 R.sub.9, CN, CONR.sub.12 R.sub.13, CH.sub.2 NR.sub.12 R.sub.13, CH.sub.2 NHCOR.sub.14, CH.sub.2 NHSO.sub.2 R.sub.17 or 5-tetrazoyl; Q.sub.3 is ##STR3## 5-tetrazolyl, CH.sub.2 CONHCOR.sub.7, COOH or certain ester, amide, carboximido or sulfonimido derivatives thereof, CONHOH, CONHCONH.sub.2, or COCH.sub.2 Q.sub.4 and Q.sub.4 is CN or COOH or certain esters thereof; R.sub.1 is hydrogen, benzyl or certain acyl groups; R.sub.4 is hydrogen, certain alkyl or certain aralkyl groups; R.sub.5 is hydrogen or certain alkyl groups; Z is (C.sub.1 -C.sub.9)alkylene, optionally interrupted by O, S, SO or SO.sub.2 ; and W is hydrogen, methyl, certain aryl or cycloalkyl groups; useful in mammals as analgesics, tranquilizers, antiemetic agents, diuretics, anticonvulsants, Antidiarrheals, antitussives, in treatment of glaucoma, and intermediates therefore.
    化学式为##STR1##的双环融合苯类化合物及其药学上可接受的阳离子和酸性加成盐,其中M为O、CH.sub.2或NR.sub.6;R.sub.6为氢、甲酰、羧苄氧或某些羧烷氧基烷基、酰基、烷基、芳基烷基或芳基烷基羰基基团;A'为:(1)当A为氢时,B为C(R.sub.2R.sub.3)(CH.sub.2).sub.fQ且f为1或2;当B为氢时,A为C(R.sub.2R.sub.3)(CH.sub.2).sub.fQ且f为0或1,当A和OR.sub.1在一起时形成内酯或其某些衍生物;(2)A'为##STR2##(3)A'为Q.sub.3;Q为CO.sub.2R.sub.7、COR.sub.8、C(OH)R.sub.8R.sub.9、CN、CONR.sub.12R.sub.13、CH.sub.2NR.sub.12R.sub.13、CH.sub.2NHCOR.sub.14、CH.sub.2NHSO.sub.2R.sub.17或5-四唑基;Q.sub.3为##STR3##5-四唑基、CH.sub.2CONHCOR.sub.7、COOH或其某些酯、酰胺、羧酸亚胺或磺酰亚胺衍生物,CONHOH、CONHCONH.sub.2或COCH.sub.2Q.sub.4,Q.sub.4为CN或COOH或其某些酯;R.sub.1为氢、苄基或某些酰基;R.sub.4为氢、某些烷基或某些芳基烷基;R.sub.5为氢或某些烷基;Z为(C.sub.1-C.sub.9)烷基,可选地由O、S、SO或SO.sub.2中断;W为氢、甲基、某些芳基或环烷基基团;在哺乳动物中作为镇痛剂、镇静剂、止吐剂、利尿剂、抗癫痫药、抗腹泻药、镇咳剂、治疗青光眼和其中间体。
  • Bicyclic benzo fused pyran compounds used for producing analgesia
    申请人:Pfizer Inc.
    公开号:US04863934A1
    公开(公告)日:1989-09-05
    Bicyclic fused benzenoid compounds of the formula ##STR1## and pharmaceutically acceptable cationic and acid addition salts thereof, where M is O, CH.sub.2 or NR.sub.6 ; R.sub.6 is hydrogen, formyl, carbobenzyloxy or certain carboalkoxyalkyl, alkanoyl, alkyl, aralkyl or aralkylcarbonyl groups; A' is: (1) A where one of A and B is hydrogen such that when A is hydrogen, B is C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q and f is 1 or 2; when B is hydrogen, A is C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q and f is 0 or 1, when taken together A and OR.sub.1 form a lactone or certain derivatives thereof; (2) A' is ##STR2## (3) A' is Q.sub.3 ; Q is CO.sub.2 R.sub.7, COR.sub.8, C(OH)R.sub.8 R.sub.9, CN, CONR.sub.12 R.sub.13, CH.sub.2 NR.sub.12 R.sub.13, CH.sub.2 NHCOR.sub.14, CH.sub.2 NHSO.sub.2 R.sub.17 or 5-tetrazoyl; Q.sub.3 is ##STR3## 5-tetrazolyl, CH.sub.2 CONHCOR.sub.7, COOH or certain ester, amide, carboximido or sulfonimido derivatives thereof, CONHOH, CONHCONH.sub.2, or COCH.sub.2 Q.sub.4 where Q.sub.4 is CN or COOH or certain esters thereof; R.sub.1 is hydrogen, benzyl or certain acyl groups; R.sub.4 is hydrogen, certain alkyl or certain aralkyl groups; R.sub.5 is hydrogen or certain alkyl groups; Z is (C.sub.1 -C.sub.9)alkylene, optionally interrupted by O, S, SO or SO.sub.2 ; and W is hydrogen, methyl, certain aryl or cycloalkyl groups; useful in mammals as analgesics, tranquilizers, antiemetic agents, diuretics, anticonvulsants, antidiarrheals, antitussives, in treatment of glaucoma, and intermediates therefore.
    公式为##STR1##的双环融合苯类化合物以及其药学上可接受的阳离子和酸加成盐,其中M为O,CH.sub.2或NR.sub.6;R.sub.6为氢,甲酰基,羧苄氧基或某些羧烷氧基烷基,烷酰基,烷基,芳基烷基或芳基烷基羰基基团;A'为:(1)A,其中A和B中的一个为氢,使得当A为氢时,B为C(R.sub.2R.sub.3)(CH.sub.2).sub.fQ,f为1或2;当B为氢时,A为C(R.sub.2R.sub.3)(CH.sub.2).sub.fQ,f为0或1,当A和OR.sub.1一起形成内酯或某些衍生物时;(2)A'为##STR2##(3)A'为Q.sub.3;Q为CO.sub.2R.sub.7,COR.sub.8,C(OH)R.sub.8R.sub.9,CN,CONR.sub.12R.sub.13,CH.sub.2NR.sub.12R.sub.13,CH.sub.2NHCOR.sub.14,CH.sub.2NHSO.sub.2R.sub.17或5-四唑基;Q.sub.3为##STR3##5-四唑基,CH.sub.2CONHCOR.sub.7,COOH或某些酯,酰胺,羧酸亚胺或磺酰亚胺衍生物,CONHOH,CONHCONH.sub.2或COCH.sub.2Q.sub.4,其中Q.sub.4为CN或COOH或某些酯;R.sub.1为氢,苄基或某些酰基;R.sub.4为氢,某些烷基或某些芳基烷基;R.sub.5为氢或某些烷基;Z为(C.sub.1-C.sub.9)烷基,可选地被O,S,SO或SO.sub.2打断;W为氢,甲基,某些芳基或环烷基团;在哺乳动物中作为镇痛剂,镇静剂,止吐剂,利尿剂,抗癫痫剂,止泻剂,止咳剂,治疗青光眼,以及其中间体。
  • Bicyclic benzo fused pyran compounds used for nausea treatment and
    申请人:Pfizer Inc.
    公开号:US04870084A1
    公开(公告)日:1989-09-26
    Bicyclic fused benzenoid compounds of the formula ##STR1## and pharmaceutically acceptable cationic and acid addition salts thereof, where M is O, CH.sub.2 or NR.sub.6 ; R.sub.6 is hydrogen, formyl, carbobenzyloxy or certain carboalkoxyalkyl, alkanoyl, alkyl, aralkyl or aralkylcarbonyl groups; A' is: (1) A where one of A and B is hydrogen such that when A is hydrogen, B is C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q and f is 1 or 2; when B is hydrogen, A is C(R.sub.2 R.sub.3)(CH.sub.2).sub.f Q and f is 0 or 1, when taken together A and OR.sub.1 form a lactone or certain derivatives thereof; (2) A' is ##STR2## (3) A' is Q.sub.3 ; Q is CO.sub.2 R.sub.7, COR.sub.8, C(OH)R.sub.8 R.sub.9, CN, CONR.sub.12 R.sub.13, CH.sub.2 NR.sub.12 R.sub.13, CH.sub.2 NHCOR.sub.14, CH.sub.2 NHSO.sub.2 R.sub.17 or 5-tetrazoyl; Q.sub.3 is ##STR3## 5-tetrazolyl, CH.sub.2 CONHCOR.sub.7, COOH or certain ester, amide, carboximido or sulfonimido derivatives thereof, CONHOH, CONHCONH.sub.2, or COCH.sub.2 Q.sub.4 where Q.sub.4 is CN or COOH or certain esters thereof; R.sub.1 is hydrogen, benzyl or certain acyl groups; R.sub.4 is hydrogen, certain alkyl or certain aralkyl groups; R.sub.5 is hydrogen or certain alkyl groups; Z is (C.sub.1 -C.sub.9) alkylene, optionally interrupted by O, S, SO or SO.sub.2 ; and W is hydrogen, methyl, certain aryl or cycloalkyl groups; useful in mammals as analgesics, tranquilizers, antiemetic agents, diuretics, anticonvulsants, antidiarrheals, antitussives, in treatment of glaucoma, and intermediates therefore.
    公式为 ##STR1## 的双环融合苯类化合物及其药学上可接受的阳离子和酸加成盐,其中M为O,CH.sub.2或NR.sub.6;R.sub.6为氢、甲酰、碳苯甲氧基或某些碳酰基烷氧基、烷酰基、烷基、芳基烷基或芳基烷基羰基基团;A'为:(1)当A为氢时,A'为A,其中A和B中的一个为氢,使得当A为氢时,B为C(R.sub.2R.sub.3)(CH.sub.2).sub.fQ,f为1或2;当B为氢时,A为C(R.sub.2R.sub.3)(CH.sub.2).sub.fQ,f为0或1,当A和OR.sub.1一起时形成内酯或某些衍生物;(2)A'为##STR2##(3)A'为Q.sub.3;Q为CO.sub.2R.sub.7,COR.sub.8,C(OH)R.sub.8R.sub.9,CN,CONR.sub.12R.sub.13,CH.sub.2NR.sub.12R.sub.13,CH.sub.2NHCOR.sub.14,CH.sub.2NHSO.sub.2R.sub.17或5-四唑基;Q.sub.3为##STR3##5-四唑基,CH.sub.2CONHCOR.sub.7,COOH或某些酯、酰胺、羧酸亚胺或磺酰亚胺衍生物,CONHOH,CONHCONH.sub.2或COCH.sub.2Q.sub.4,其中Q.sub.4为CN或COOH或某些酯;R.sub.1为氢、苄基或某些酰基;R.sub.4为氢、某些烷基或某些芳基烷基;R.sub.5为氢或某些烷基;Z为(C.sub.1-C.sub.9)烷基,可选地由O、S、SO或SO.sub.2中断;W为氢、甲基、某些芳基或环烷基基团;在哺乳动物中作为镇痛剂、镇静剂、止吐剂、利尿剂、抗癫痫剂、止泻剂、镇咳剂、治疗青光眼和其中间体。
  • US4486428A
    申请人:——
    公开号:US4486428A
    公开(公告)日:1984-12-04
  • US4680404A
    申请人:——
    公开号:US4680404A
    公开(公告)日:1987-07-14
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