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8-(3,4-dimethylphenyl)-1,5-dimethyl-5,6-dihydro-1H-pyrrolo[3,2-c]azepin-4-one | 1193523-67-9

中文名称
——
中文别名
——
英文名称
8-(3,4-dimethylphenyl)-1,5-dimethyl-5,6-dihydro-1H-pyrrolo[3,2-c]azepin-4-one
英文别名
8-(3,4-dimethylphenyl)-1,5-dimethyl-6H-pyrrolo[3,2-c]azepin-4-one
8-(3,4-dimethylphenyl)-1,5-dimethyl-5,6-dihydro-1H-pyrrolo[3,2-c]azepin-4-one化学式
CAS
1193523-67-9
化学式
C18H20N2O
mdl
——
分子量
280.37
InChiKey
HWFCHCPWZQTOGF-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):
    2.4
  • 重原子数:
    21
  • 可旋转键数:
    1
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    25.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    1-methyl-1H-pyrrole-2-carboxylic acid [3-(3,4-dimethylphenyl)prop-2-ynyl]methylamidedihydrogen hexachloroplatinate(IV) hexahydrate 作用下, 以 甲苯 为溶剂, 反应 20.0h, 以75%的产率得到8-(3,4-dimethylphenyl)-1,5-dimethyl-5,6-dihydro-1H-pyrrolo[3,2-c]azepin-4-one
    参考文献:
    名称:
    铂催化炔烃的分子内环化:吡咯并ze庚醌衍生物的高效合成
    摘要:
    实现封闭:铂催化的环异构化反应(参见方案; [Pd / Cu] = [PdCl 2(PPh 3)2 ] / CuI,Ar =芳基,X = Br,I)可用于生物的高效直接合成相关的吡咯并[3,2 – c ] azepin-4-one衍生物。
    DOI:
    10.1002/anie.200902937
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文献信息

  • Platinum-Catalyzed Intramolecular Cyclizations of Alkynes: Efficient Synthesis of Pyrroloazepinone Derivatives
    作者:Marina Gruit、Dirk Michalik、Annegret Tillack、Matthias Beller
    DOI:10.1002/anie.200902937
    日期:2009.9.14
    Achieving closure: A platinum‐catalyzed cycloisomerization reaction (see scheme; [Pd/Cu]=[PdCl2(PPh3)2]/CuI, Ar=aryl, X=Br,I) is used for the efficient straightforward synthesis of biologically relevant pyrrolo‐[3,2‐c]azepin‐4‐one derivatives.
    实现封闭:铂催化的环异构化反应(参见方案; [Pd / Cu] = [PdCl 2(PPh 3)2 ] / CuI,Ar =芳基,X = Br,I)可用于生物的高效直接合成相关的吡咯并[3,2 – c ] azepin-4-one衍生物。
  • Synthesis of pyrroloazepinones: platinum- and gold-catalyzed cyclization reactions of alkynes
    作者:Marina Gruit、Dirk Michalik、Karolin Krüger、Anke Spannenberg、Annegret Tillack、Anahit Pews-Davtyan、Matthias Beller
    DOI:10.1016/j.tet.2010.02.091
    日期:2010.5
    The synthesis of potentially bioactive pyrroloazepinones based on the catalytic intramolecular cyclization of alkyne-substituted 1H-pyrrole-2-carboxylic acid amides has been developed. In the presence of either H2PtCl6·6H2O at 120 °C or AuCl3 at room temperature pyrrolo[3,2-c]azepin-4-ones are formed.
    已经开发了基于炔烃取代的1 H-吡咯-2-羧酸酰胺的催化分子内环化反应的潜在生物活性吡咯并ze庚酮的合成方法。在120°C下存在H 2 PtCl 6 ·6H 2 O或在室温下存在AuCl 3的情况下,会生成吡咯并[3,2 - c ] azepin-4-ones。
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同类化合物

环戊二烯并[4,5]氮杂卓并[2,1,7-cd]吡咯里嗪 吡咯并[1,2-a]氮杂-5-酮 六氢-1H-吡咯并[1,2-A]氮杂卓-5(6H)-酮 N,N-二甲基-3-(3-甲基-1,2,4,5-四氢氮杂卓并[4,5-b]吲哚-6-基)丙-1-胺 9-氟-1,2,3,4,5,6-六氢氮杂卓并[4,5-b]吲哚 7,8-二氢-5H-吡咯并[1,2-A]氮杂环庚烷-9(6H)-酮 6-叔-丁基3A-乙基八氢吡咯并[2,3-D]氮杂卓-3A,6(2H)-二甲酸基酯 6,7-二氢吡咯并[2,3-c]氮杂卓-4,8(1H,5H)-二酮 5H-吡咯并[1,2-a]氮杂卓-7-醇 5,9:7,11-二亚甲基-5H-吡咯并[1,2-a]吖壬英-3-羧酸,6,7,8,9,10,11-六氢-,甲基酯 4-(2-氨基-1H-咪唑-5-基)-2,3-二溴-6,7-二氢吡咯并[2,3-c]氮杂卓-8(1H)-酮 4-(2-氨基-1H-咪唑-4-基)-2,3-二溴-4,5,6,7-四氢吡咯并[2,3-c]氮杂卓-8(1H)-酮 4-(2-氨基-1,5-二氢-5-氧代-4H-咪唑-4-亚基)-4,5,6,7-四氢-吡咯并[2,3-c]氮杂卓-8(1H)-酮 3-苄基-1,2,3,4,5,6-六氢氮杂卓并[4,5-b]吲哚 3-(3,9-二甲基-1,2,4,5-四氢氮杂卓并[4,5-b]吲哚-6-基)-N,N-二甲基丙烷-1-胺 2H,3H-氧杂环丁烷并[3,2-d]吡咯并[1,2-a]氮杂卓 2-溴-6,7-二氢-1h,5h-吡咯并[2,3-c]氮杂烷-4,8-二酮 2,5-已炔二醇 2,3,4,5-四氢-N,N-二甲基-2-(3,4,5-三甲氧基苯甲酰基)-氮杂卓并(3,4-b)吲哚-10(1H)-丙胺 11-氧杂-3,10-二氮杂三环[7.2.1.03,7]十二碳-1,4,6,9-四烯 1,4,5,6,7,8-六氢吡咯并[3,2-b]氮杂卓 1,2,3,4,5,6-六氢氮杂环庚烷[4,3-B]吲哚盐酸盐 1,2,3,4,5,6-六氢-9-甲基氮杂卓并[4,5-b]吲哚 1,2,3,4,5,6-六氢-6-甲基氮杂革[4,5-b]吲哚盐酸盐 1,2,3,4,5,6-六氢-3-甲基氮杂卓并[4,5-b]吲哚 (1R*,2E,11S*)-2-(cyclohexylmethylene)-1-(phenylsilyl)methyloctahydropyrrolo[1,2-a]azepine (R)-2-(6,7,8,9-tetrahydro-5H-pyrrolo[1,2-a]azepin-9-yl)-acetaldehyde curvulamine (3aR,8aS)-tert-butyl octahydropyrrolo[3,4-d]azepine-2(1H)-carboxylate hydrochloride tert-butyl 6-(2-amino-2-oxoethyl)-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate 3-benzoyl-10-bromo-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole 3-(tert-butyloxycarbonyl)-10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole 1,2,3,4,5,6-hexahydro-3-dimethylaminoethyl-5-hydroxymethylazepino[4,5-b]indole 1,2,3,4,5,6-hexahydro-3-dimethylaminoethyl-5-hydroxymethyl-6-methylazepino[4,5-b]indole (Z)-2,3,9,9a-tetrahydro-6,6-dimethyl-9-methylene-8-vinyl-1H-pyrrolo[1,2-a]azepin-5(6H)-one 2,3,4,5,6,7-hexahydro-1H-3a,8,13,13b-tetraazabenzo[b]cyclopenta[1,2,3-jk]fluorene 2,3,4,5,6,7-hexahydro-1H-3a,8,11,11b-tetraazacyclohepta[1,2,3-jk]fluorene 1-Benzyloxy-2-methoxy-7,8,9,10-tetrahydro-6H-azepino<1,2-a>indole-11-carbaldehyde 3-benzoyl-10-(2-propoxyphenyl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole 2-phenyl-2,4,5,6-tetrahydro-1H-6-azabenzo[a]cyclohepta[cd]azulen-1-one 2-carbetoxy-3-(N,N-dimethyl)aminomethyleneamino-8-oxo-8H-4,5,6,7-tetrahydropyrrolo<2,3-c>azepine 3-benzoyl-10-[2-(trifluoromethyl)phenyl]-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole 3-benzoyl-10-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole 6-[2-(4-fluorophenyl)ethyl]-3,4,5,6-tetrahydroazepino[4,3-b]indol-1(2H)-one 5-(2-hydroxy-3-morpholin-4-yl-propyl)-3-methyl-4-oxo-1,4,5,6,7,8-hexahydro-pyrrolo[3,2-c]azepine-2-carbaldehyde 6-(2-phenylethyl)-3,4,5,6-tetrahydroazepino[4,3-b]indol-1(2H)-one 11-(tert-butyldimethylsilyloxy)-1-trimethylsilyl-3a,4,11,12-tetrahydro-3H-cyclopenta[5,6]azepine[1,2-a]indole-2-one tert-butyl 8,9-dichloro-6-[2-(2,3-dimethylanilino)-2-oxoethyl]-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate tert-butyl 9,10-dichloro-6-[2-(2,3-dimethylanilino)-2-oxoethyl]-1,4,5,6-tetrahydroazepino[4,5-b]indole-3(2H)-carboxylate tert-butyl (1R,4S)-1-(benzylcarbamoyl)-3-oxo-2-((S)-1-phenylethyl)-1,2,3,4,5,10-hexahydroazepino[3,4-b]indol-4-ylcarbamate