摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(1,1-dioxo-1λ6-thietan-3-yl)amine trifluoroacetate | 1331887-01-4

中文名称
——
中文别名
——
英文名称
(1,1-dioxo-1λ6-thietan-3-yl)amine trifluoroacetate
英文别名
1,1-dioxo-thietan-3-ylamine trifluoroacetate;1,1-dioxidethietan-3ylamine trifluoroacetate;1,1-Dioxothietan-3-amine;2,2,2-trifluoroacetic acid
(1,1-dioxo-1λ<sup>6</sup>-thietan-3-yl)amine trifluoroacetate化学式
CAS
1331887-01-4
化学式
C2HF3O2*C3H7NO2S
mdl
——
分子量
235.184
InChiKey
BPSQARQJGHFZGB-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):
    -0.62
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.8
  • 拓扑面积:
    106
  • 氢给体数:
    2
  • 氢受体数:
    8

反应信息

点击查看最新优质反应信息

文献信息

  • PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES
    申请人:Syngenta Participations AG
    公开号:US20160073631A1
    公开(公告)日:2016-03-17
    The present invention provides stereoselective processes for the preparation of compounds of formula (I) wherein P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; R 1 is chlorodifluoromethyl or trifluoromethyl; R 2 is optionally substituted aryl or optionally substituted heteroaryl; n is 0 or 1; including the process comprising (a-i) reacting a compound of formula II wherein P, R 1 and R 2 are as defined for the compound of formula I; with nitromethane in the presence a chiral catalyst to give a compound of formula III wherein P, R 1 and R 2 are as defined for the compound of formula I; and (a-ii) reductively cyclising the compound of formula III to give the compound of formula I. The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).
    本发明提供了用于制备式(I)化合物的立体选择性过程,其中 P为苯基、基、含有一个或两个氮原子作为环成员的6元杂芳基,或含有一个或两个氮原子作为环成员的10元双环杂芳基,其中苯基、基和杂芳基可以选择性地被取代; R1为甲基或三甲基; R2为可以选择性取代的芳基或可以选择性取代的杂芳基; n为0或1; 包括以下过程 (a-i)将式II化合物与硝基甲烷在手性催化剂存在下反应,得到式III化合物; 其中P、R1和R2如式I化合物中所定义; (a-ii)将式III化合物还原环化,得到式I化合物。 本发明还提供了用于合成式(I)化合物的过程的中间体。
  • [EN] DIHYDROFURAN DERIVATIVES AS INSECTICIDAL COMPOUNDS<br/>[FR] DÉRIVÉS DE DIHYDROFURANE EN TANT QUE COMPOSÉS INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2013026724A1
    公开(公告)日:2013-02-28
    The present invention relates to compounds of formula (IA) wherein QA is QA1 or QA2 P is P1, heterocyclyl or heterocyclyl substituted by one to five Z; and wherein A1, A2, A3, A4, G1, Z, R1, R2, R3 and R4 are as defined in claim 1; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (IA), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (IA) and to methods of using the compounds of formula (IA) to control insect, acarine, nematode and mollusc pests.
    本发明涉及式(IA)的化合物,其中QA是QA1或QA2,P是P1,杂环烷基或被1至5个Z取代的杂环烷基;以及其中A1、A2、A3、A4、G1、Z、R1、R2、R3和R4如权利要求1所定义;或其盐或N-氧化物。此外,本发明涉及制备式(IA)化合物的过程和中间体,包括含有式(IA)化合物的杀虫剂杀螨剂、杀线虫剂和杀软体动物剂组合物,以及使用式(IA)化合物控制昆虫、螨虫、线虫和软体动物害虫的方法。
  • DIHYDROFURAN DERIVATIVES AS INSECTICIDAL COMPOUNDS
    申请人:El Qacemi Myriem
    公开号:US20120329769A1
    公开(公告)日:2012-12-27
    The present invention relates to compounds of formula (I) wherein Q is Q1 or Q2 P is P1, heterocyclylor heterocyclyl substituted by one to five Z; and wherein A 1 , A 2 , A 3 , A 4 , G 1 , Y 1 , Z, R 1 , R 2 , R 3 and R 4 are as defined in claim 1 ; or a salt or N-oxide thereof. Furthermore, the present invention relates to processes and intermediates for preparing compounds of formula (I), to insecticidal, acaricidal, nematicidal and molluscicidal compositions comprising the compounds of formula (I) and to methods of using the compounds of formula (I) to control insect, acarine, nematode and mollusc pests.
    本发明涉及式(I)的化合物,其中Q为Q1或Q2,P为P1,杂环烷基或被1至5个Z取代的杂环烷基;以及其中A1、A2、A3、A4、G1、Y1、Z、R1、R2、R3和R4如权利要求1所定义;或其盐或N-氧化物。此外,本发明涉及制备式(I)化合物的过程和中间体,含有式(I)化合物的杀虫剂杀螨剂、杀线虫剂和杀软体动物剂组合物,以及使用式(I)化合物控制昆虫、螨虫、线虫和软体动物害虫的方法。
  • [EN] PROCESS FOR THE PREPARATION OF DIHYDROPYRROLE DERIVATIVES<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION DE DÉRIVÉS DE DIHYDROPYRROLE
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2011154555A1
    公开(公告)日:2011-12-15
    The present invention provides stereoselective processes for the preparation of compounds of formula (I) wherein P is phenyl, naphthyl, a 6-membered heteroaryl group containing one or two nitrogen atoms as ring members, or a 10-membered bicyclic heteroaryl group containing one or two nitrogen atoms as ring members, and wherein the phenyl, naphthyl and heteroaryl groups are optionally substituted; R1 is chlorodifluoromethyl or trifluoromethyl; R2 is optionally substituted aryl or optionally substituted heteroaryl; n is 0 or 1; including the process comprising (a-i) reacting a compound of formula II wherein P, R1 and R2 are as defined for the compound of formula I; with nitromethane in the presence a chiral catalyst to give a compound of formula III Wherein P, R1 and R2 are as defined for the compound of formula I; and (a-ii) reductively cyclising the compound of formula III to give the compound of formula I. The invention also provides intermediates useful for processes for the synthesis of compounds of formula (I).
    本发明提供了立体选择性的制备式(I)化合物的方法,其中P是苯基、基、含有一个或两个氮原子作为环成员的6元杂环芳基基团或含有一个或两个氮原子作为环成员的10元双环杂环芳基基团,其中苯基、基和杂环芳基基团可选地被取代;R1是甲基或三甲基;R2是可选地被取代的芳基或可选地被取代的杂环芳基;n为0或1;包括以下步骤的方法:(a-i)反应式II化合物,其中P、R1和R2如式(I)化合物所定义;与硝甲烷在手性催化剂的存在下反应,得到式III化合物,其中P、R1和R2如式(I)化合物所定义;以及(a-ii)还原环化式III化合物,得到式(I)化合物。本发明还提供了用于合成式(I)化合物的中间体。
查看更多