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ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino]-4-oxo-3-phenyl-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate

中文名称
——
中文别名
——
英文名称
ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino]-4-oxo-3-phenyl-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate
英文别名
ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidene)methylamino]-4-oxo-3-phenylthieno[3,4-d]pyridazine-1-carboxylate
ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino]-4-oxo-3-phenyl-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate化学式
CAS
——
化学式
C24H23N3O5S
mdl
——
分子量
465.53
InChiKey
SFEYMPGJYMYMMG-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):
    3.88
  • 重原子数:
    33.0
  • 可旋转键数:
    5.0
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    107.36
  • 氢给体数:
    1.0
  • 氢受体数:
    9.0

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

  • 作为产物:
    描述:
    2-dimethylaminomethylene-5,5-dimethylcyclohexane-1,3-dioneethyl 5-amino-3,4-dihydro-4-oxo-3-phenylthieno<3,4-d>pyridazine-1-carboxylate溶剂黄146 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 0.02h, 以63%的产率得到ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino]-4-oxo-3-phenyl-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate
    参考文献:
    名称:
    缩合氨基噻吩的研究:微波加热下缩合氨基噻吩对弱电子和乙炔的反应性的进一步研究
    摘要:
    aminothienopyridazines的反应8A,8B,aminothienocoumarin 13和aminothienonaphthopyran 14与烯胺酮9,17和20A,B在微波辐射下,得到两个都缩合的混合物C-1烷基化产物15和16只有一个或氨基部分烷基化和二乙胺去除或这些产物的种类取决于噻吩环上取代基的性质。另一方面,这些缩合的氨基噻吩与3-二甲基氨基丙烯醛的反应得到24和25。
    DOI:
    10.1002/jhet.5570430306
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文献信息

  • Studies with condensed aminothiophenes: Further investigation on the reactivity of condensed aminothiophenes toward electron poor and acetylenes under microwave heating
    作者:Balkis Al-Saleh、Morsy A. El-Apasery
    DOI:10.1002/jhet.5570430306
    日期:2006.5
    The reaction of aminothienopyridazines 8a,b, aminothienocoumarin 13 and aminothienonaphthopyran 14 with enaminones 9, 17 and 20a,b under microwave irradiation affords either a mixture of both condensations C-1 alkylation products 15 and 16 or amino moiety alkylation and diethylamine elimination or only one of these products depending on nature of substituents on the thiophene ring. On the other hand
    aminothienopyridazines的反应8A,8B,aminothienocoumarin 13和aminothienonaphthopyran 14与烯胺酮9,17和20A,B在微波辐射下,得到两个都缩合的混合物C-1烷基化产物15和16只有一个或氨基部分烷基化和二乙胺去除或这些产物的种类取决于噻吩环上取代基的性质。另一方面,这些缩合的氨基噻吩与3-二甲基氨基丙烯醛的反应得到24和25。
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同类化合物

噻吩并[3,4-d]哒嗪-1-羧酸,5-氨基-3,4-二氢-3-(4-甲基苯基)-4-羰基-,乙基酯 1,4-二氯噻吩并[3,4-d]哒嗪 ethyl 5-[(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino]-4-oxo-3-phenyl-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5,7-Dimethyl-thieno<3,4-d>pyridazin ethyl 5-amino-3-(4-bromophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 3-(3-chlorophenyl)-5-(N-methylacetamido)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-amino-4-oxo-3-(4-(trifluoromethoxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5-amino-N-isopropyl-4-oxo-3-(4-(trifluoromethoxy)-phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-4-oxo-3-(4-(trifluoromethoxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid 5-amino-3-(4-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carbohydrazide ethyl 5-amino-3-(2-chlorophenyl)-4-oxo-3,4-dihydrothieno-[3,4-d]pyridazine-1-carboxylate 7-amino-2-(4-chlorophenyl)-4-methylthieno[3,4-d]pyridazin-1(2H)-one 7-amino-4-methylthieno[3,4-d]pyridazin-1(2H)-one ethyl 5-amino-3-(4-fluorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 7-amino-4-methyl-2-(pyridin-3-yl)thieno[3,4-d]pyridazin-1(2H)-one 7-amino-2-benzyl-4-methylthieno[3,4-d]pyridazin-1(2H)-one 7-amino-4-methyl-2-(2,2,2-trifluoroethyl)thieno[3,4-d]pyridazin-1(2H)-one 7-amino-4-methyl-2-(pyridin-2-yl)thieno[3,4-d]pyridazin-1(2H)-one N,N-dimethyl-N'-(7-methyl-4-oxo-3-p-tolyl-1-p-tolylazo-3,4-dihydrothieno[3,4-d]pyridazin-5-yl)-formamidine ethyl 5-amino-4-oxo-3-(o-tolyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 7-amino-2-isopropyl-4-methylthieno[3,4-d]pyridazin-1(2H)-one ethyl 5-amino-4-oxo-3-(4-(trifluoromethylsulfonyloxy)phenyl)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-amino-3-(4-bromophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5-amino-3-(4-chlorophenyl)-N-methyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-(4-chlorophenyl)-N,N-dimethyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-3,4-dihydro-3-p-tolylthieno<3,4-d>-pyridazin-1-carboxylic acid hydrazide 7-amino-2-cyclohexyl-4-methylthieno[3,4-d]pyridazin-1(2H)-one 5-amino-3-(4-hydroxyphenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid ethyl 5-amino-3-(4-hydroxyphenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 7-amino-2-p-tolyl-2H-thieno[3,4-d]pyridazin-1-one <3,4-d>-Thienopyridazin 5-amino-3-(3-chlorophenyl)-N-isopropyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide ethyl 5-amino-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno-[3,4-d]pyridazine-1-carboxylate 5-amino-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid ethyl 5-(butylamino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate butyl 5-(butylamino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 3-(3-chlorophenyl)-4-oxo-5-(2,2,2-trifluoroacetamido)-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-((tert-butoxycarbonyl)amino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 5-(benzylamino)-3-(3-chlorophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate ethyl 3-(3-chlorophenyl)-5-(methylamino)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylate 5-amino-3-(4-bromophenyl)-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxylic acid 5-amino-3-(4-bromophenyl)-N-isopropyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-[4-(3-(18F)fluoranylpropoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide tert-butyl N-[3-[4-(2-fluoroethoxy)phenyl]-4-oxo-1-(propan-2-ylcarbamoyl)thieno[3,4-d]pyridazin-5-yl]carbamate tert-butyl N-[3-(4-hydroxyphenyl)-4-oxo-1-(propan-2-ylcarbamoyl)thieno[3,4-d]pyridazin-5-yl]carbamate 5-amino-3-[4-(3-fluoro-2-hydroxypropoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide Tert-butyl 5-amino-3-[4-(2-fluoroethoxy)phenyl]-4-oxothieno[3,4-d]pyridazine-1-carboxylate 5-amino-3-[4-(3-fluoropropoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-[4-(2-(18F)fluoranylethoxy)phenyl]-4-oxo-N-propan-2-ylthieno[3,4-d]pyridazine-1-carboxamide 5-amino-3-(4-chlorophenyl)-N-cyclopropyl-4-oxo-3,4-dihydrothieno[3,4-d]pyridazine-1-carboxamide