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selenophene-2-carbonyl azide | 319448-11-8

中文名称
——
中文别名
——
英文名称
selenophene-2-carbonyl azide
英文别名
Selenophene-2-carbonyl azide
selenophene-2-carbonyl azide化学式
CAS
319448-11-8
化学式
C5H3N3OSe
mdl
——
分子量
200.058
InChiKey
DRVZOALMKRNVRH-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):
    1.19
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    31.4
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:e06c0cd41f162daadb94c6060fb7e1ec
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反应信息

  • 作为反应物:
    描述:
    亞甲去甲selenophene-2-carbonyl azide氘代氯仿 为溶剂, 以73%的产率得到(selenophen-2-yl)(6-methylene-2-azatricyclo[3.2.1.02,4]octan-3-yl)methanone
    参考文献:
    名称:
    The role of the carbonyl group in the intermolecular 1,3-cycloaddition of azido(2-heteroaryl)methanones with activated olefins
    摘要:
    将叠氮(2-杂芳)甲酮1–5与甲基(E)-3-吡咯烷丙-2-烯酸酯在室温下反应,生成了甲基1,2,3-三唑羧酸酯6和(2-杂芳)(吡咯烷)甲酮1a–5,通过一种不寻常的1,3-环加成反应。与极性烯烃甲基克罗纳酸酯、甲基丙炔酸酯或甲基丁-2-炔酸酯进行的叠氮甲酮1和2的类似反应未能成功。相反,受到应变的5-亚甲基双环[2.2.1]庚-2-烯与羰基叠氮化合物1–5平稳反应,生成了三唑啉加合物,随后通过失去分子氮形成了(2-杂芳)(6-亚甲基-3-氮杂三环[3.2.1.0]辛烷-3-基)甲酮1b–5b。
    DOI:
    10.1039/b203577d
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文献信息

  • The role of the carbonyl group in the intermolecular 1,3-cycloaddition of azido(2-heteroaryl)methanones with activated olefins
    作者:Paolo Zanirato
    DOI:10.1039/b203577d
    日期:2002.6.7
    Treatment of the azido(2-heteroaryl)methanones 1–5 with methyl (E)-3-pyrrolidinoprop-2-enoate at room temperature yielded the methyl 1,2,3-triazolecarboxylate 6 and (2-heteroaryl) (pyrrolidino)methanones 1a–5avia an unusual 1,3-cycloaddition reaction. Analogous reactions of the azidomethanones 1 and 2 with the dipolarophiles methyl crotonate, methyl propiolate or methyl but-2-ynoate failed. In contrast, the strained 5-methylenebicyclo[2.2.1]hept-2-ene reacted smoothly with the carbonyl azides 1–5 to give triazoline adducts which subsequently formed the (2-heteroaryl)(6-methylene-3-azatricyclo[3.2.1.0]octan-3-yl)methanones 1b–5b by loss of molecular nitrogen.
    将叠氮(2-杂芳)甲酮1–5与甲基(E)-3-吡咯烷丙-2-烯酸酯在室温下反应,生成了甲基1,2,3-三唑羧酸酯6和(2-杂芳)(吡咯烷)甲酮1a–5,通过一种不寻常的1,3-环加成反应。与极性烯烃甲基克罗纳酸酯、甲基丙炔酸酯或甲基丁-2-炔酸酯进行的叠氮甲酮1和2的类似反应未能成功。相反,受到应变的5-亚甲基双环[2.2.1]庚-2-烯与羰基叠氮化合物1–5平稳反应,生成了三唑啉加合物,随后通过失去分子氮形成了(2-杂芳)(6-亚甲基-3-氮杂三环[3.2.1.0]辛烷-3-基)甲酮1b–5b。
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同类化合物

硒酚 硒吩并[3,2-B]噻吩 硒吩-3-羧酸 硒吩-2-羧酸 硒吩-2-硼酸 5-甲基-2-硒吩羰基氯化物 5-甲基-2-硒吩亚磺酸 3-硒吩羰基氯化物 3-甲基硒吩 3,4-双(氯甲基)-2,5-二甲基硒吩 2-甲基-硒吩 2-乙烯基硒吩 2,5-二-(2'-噻吩基)硒吩 2,2'-双硒 2,6-di(selenophen-2-yl)tetrahydro-4H-selenopyran-4-one 2-(2-(selenophen-2-yl)ethynyl)selenophene (2-selenophene-2-yl)lithium 2-(dec-1-ynyl)selenophene (3-selenienyl)di(1-adamantyl)methanol 5-Methyl-2-mercapto-selenophen seleno[3,4-b]thiophene 3-Selenophenethiol, 2,5-dimethyl- 2-dicyanomethylselenophene bis(3-selenienyl)methanol 2-Propyl-selenophen 2-(5'-hydroxymethyl-2'-selenyl)-thiophene 4,4,6,6-tetramethyl-2-{[(methylsulfonyl)thio]methyl}-4,6-dihydro-5H-selenolo[2,3-c]pyrrol-5-yloxyl radical selenosulflower 5-Carboxyseleno<2,3-b>thiophen methyl 4-[(dimethylamino)diazenyl]-5-methylselenophene-2-carboxylate ethyl selenopheno[3,2-b]thiophene-5-carboxylate 3-Cyanoselenophen 2,4-Ditert-butylselenophene 5-Hydroxymethyl-selenophen-2-carbonsaeure 1,3-Dithiolo<4,5-c>selenophene-2-thione methyl 3-amino-5-(methoxycarbonyl)selenophene-2-carboxylate tetramethyl 2,3,4,5-selenophenetetracarboxylate 2,2'-{5,5'-[5,5'-(selenophene-2,5-diyl)bis(3,4-dibutylthien-5,2-diyl)]bis-(selenophene-5,2-diyl)}bis(methan-1-yl-1-ylidene)dimalononitrile 2-(2-bromoethylsulfonyl)selenophene 2-(4,4-bis(methoxymethyl)-7-(selenophen-2-yl)hepta-1,6-diynyl)selenophene cyclopenta[c]selenophene-(CH2OMe)2 2-[5,5-Bis(methoxymethyl)-3-thiophen-2-yl-4,6-dihydrocyclopenta[c]selenophen-1-yl]thiophene 3,6-dimethylselenolo<3,2-b>selenophene 2,5-Bis(2-selenienyl)furan tetramethyl-selenophene 2,3,4-trimethyl-selenophene 2,3,5-trimethyl-selenophene selenophen-2-yl-methanol 1-selenophen-2-yl-ethanol 2-carbomethoxyselenophene