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2-(thietan-3-ylidene)acetonitrile | 61890-05-9

中文名称
——
中文别名
——
英文名称
2-(thietan-3-ylidene)acetonitrile
英文别名
——
2-(thietan-3-ylidene)acetonitrile化学式
CAS
61890-05-9
化学式
C5H5NS
mdl
——
分子量
111.167
InChiKey
YGQIAWYMABKWPN-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):
    0.1
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    49.1
  • 氢给体数:
    0
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2934999090

SDS

SDS:b0b4852abf42364e4802a0edca6bb5a0
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反应信息

  • 作为反应物:
    描述:
    2-(thietan-3-ylidene)acetonitrile甲醇 、 sodium tetrahydroborate 、 potassium phosphate 、 hydrido(dimethylphosphinous acid-κP)[hydrogen bis(dimethylphosphinito-κP)]platinum(II) 、 [(2-di-tert-butylphosphino-2′,4′,6′-triisopropyl-1, 1′-biphenyl)-2-(2′-amino-1,1′-biphenyl)] palladium(II) methanesulfonate 、 氨基磺酸双氧水 作用下, 以 1,4-二氧六环乙醇乙腈 为溶剂, 反应 50.5h, 生成 (1S,8R)-5-(2,6-difluoro-phenyl)-1-{6-[3-(1,1-dioxo-1λ6-thietan-3-ylmethyl)-[1,2,4]triazol-1-yl]-4-methyl-pyridin-2-yl}-11,11-dimethyl-3,4-diaza-tricyclo[6.2.1.02,7]undeca-2(7),3,5-triene
    参考文献:
    名称:
    [EN] PYRIDAZINE DERIVATIVES AS RORC MODULATORS
    [FR] DÉRIVÉS DE PYRIDAZINE UTILISÉS EN TANT QUE MODULATEURS DE RORC
    摘要:
    式(I)的化合物或其药用盐,其中m、n、p、q、A、B、R1、R2、R3、R4、R5、R6和R7如本文所定义。还公开了制备这些化合物的方法,并将这些化合物用作RORs调节剂,用于治疗炎症性疾病,如关节炎。
    公开号:
    WO2018083105A1
  • 作为产物:
    描述:
    3-硫杂环丁酮(三苯基膦)乙腈二氯甲烷 为溶剂, 以785 mg的产率得到2-(thietan-3-ylidene)acetonitrile
    参考文献:
    名称:
    [EN] ISOXAZOLINE DERIVATIVES AS INSECTICIDAL COMPOUNDS
    [FR] DÉRIVÉS D'ISOXAZOLINE EN TANT QUE COMPOSÉS INSECTICIDES
    摘要:
    本发明提供了以下式(I)的化合物,其中G1为氧;R1为氢;R2为P基团;L为键合,亚甲基或乙烯基;A1和A2中的一个为S、SO或SO2,另一个为-C(R4)R4-;R3为氢或甲基;每个R4独立地为氢或甲基;Y1、Y2和Y3独立地为CH或氮;其中Y1、Y2和Y3中不超过两个为氮,且Y2和Y3不同时为氮;R5为氯、溴或氟;X2为C-X6或氮;Χ1、Χ3和X6独立地为氢、卤素或三卤甲基,其中至少两个X1、X3和X6不为氢;X4为三氟甲基、二氟甲基或氯二氟甲基。该发明还涉及使用这些化合物来控制昆虫、蜱、线虫或软体动物的方法,以及用于合成这些化合物的中间体。
    公开号:
    WO2013026695A1
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文献信息

  • [EN] PROCESS FOR THE PREPARATION OF THIETANE DERIVATIVES<br/>[FR] PROCÉDÉ DE PRÉPARATION DE DÉRIVÉS DE THIÉTANE
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2013026930A1
    公开(公告)日:2013-02-28
    The present invention relates to processes for the preparation of thietane derivatives of the formula (IA) and thietane derivatives of the formula (IB) wherein R1, R2, A1, A2, A3, A4, B, and n are as defined in the claims. The invention also relates to intermediates useful in the processes, as well as the compounds of formula (IA) and (IB) and their use as pesticides.
    本发明涉及制备式(IA)的噻环烷衍生物和式(IB)的噻环烷衍生物的过程,其中R1、R2、A1、A2、A3、A4、B和n如权利要求中所定义。该发明还涉及在该过程中有用的中间体,以及式(IA)和(IB)的化合物及其作为杀虫剂的用途。
  • [EN] DIHYDROPYRROLE DERIVATIVES AS INSECTICIDAL COMPOUNDS<br/>[FR] DÉRIVÉS DE DIHYDROPYRROLE EN TANT QUE COMPOSÉS INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2013026929A1
    公开(公告)日:2013-02-28
    The present invention provides compounds of formula (I), wherein G1 is oxygen; R1 is hydrogen; R2 is group P L is a bond, methylene or ethylene; one of A1 and A2 is S, SO or S02 and the other is -C(R4)R4- R3 is hydrogen or methyl; each R4 is independently hydrogen or methyl; Y1 is C-R6, CH or nitrogen; Y2 and Y3 are independently CH or nitrogen; wherein no more than two of Y1, Y2 and Y3 are nitrogen and wherein Y2 and Y3 are not both nitrogen; R5 is hydrogen, halogen, cyano, nitro, NH2, -C2alkyl, C3-C2haloalkyl, C3-C5cycloalkyl, C3- C5halocycloalkyl, C1-C2alkoxy, C1-C2haloalkoxy; R6 together with R5 forms a -CH=CH-CH=CH- bridge; X2 is C-X6 or nitrogen; X1, X3 and X6 are independently hydrogen, halogen or trihalomethyl, wherein at least two of X1, X3 and X6 are not hydrogen; X4 is trifluoromethyl, difluoromethyl or chlorodifluoromethyl. The invention also provides intermediates useful for the preparation of compounds of formula I, as well as methods of controlling insects, acarines, nematodes or molluscs using the compounds of formula I.
    本发明提供了式(I)的化合物,其中G1为氧;R1为氢;R2为P基团;L为键,亚甲基或乙烯基;A1和A2中的一个为S,SO或S02,另一个为-C(R4)R4-;R3为氢或甲基;每个R4独立地为氢或甲基;Y1为C-R6,CH或氮;Y2和Y3独立地为CH或氮;其中Y1、Y2和Y3中不超过两个为氮,且Y2和Y3不同时为氮;R5为氢、卤素、氰基、硝基、NH2、-C2烷基、C3-C2卤代烷基、C3-C5环烷基、C3-C5卤代环烷基、C1-C2烷氧基、C1-C2卤代烷氧基;R6与R5一起形成一个-CH=CH-CH=CH-桥;X2为C-X6或氮;X1、X3和X6独立地为氢、卤素或三卤甲基,其中至少两个不是氢;X4为三氟甲基、二氟甲基或氯二氟甲基。本发明还提供了用于制备式(I)化合物的中间体,以及使用式(I)化合物控制昆虫、螨虫、线虫或软体动物的方法。
  • [EN] ISOXAZOLINE DERIVATIVES AS INSECTICIDAL COMPOUNDS<br/>[FR] DÉRIVÉS D'ISOXAZOLINE CONVENANT COMME COMPOSÉS INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2013026931A1
    公开(公告)日:2013-02-28
    The present invention provides compounds of formula (I), wherein G1 is oxygen; R1 is hydrogen; R2 is group P (P) L is a bond, methylene or ethylene; one of A1 and A2 is S, SO or SO2 and the other is -C(R4)R4-R3 is hydrogen or methyl; each R4 is independently hydrogen or methyl; Y1 is C-R6, CH or nitrogen; Y2 and Y3 are independently CH or nitrogen; wherein no more than two of Y1, Y2 and Y3 are nitrogen and wherein Y2 and Y3 are not both nitrogen; R5 is hydrogen, halogen, cyano, nitro, NH2, C1-C2alkyl, C1-C2haloalkyl, C3-C5cycloalkyl, C3-C5halocycloalkyl, C1-C2alkoxy, C1-C2haloalkoxy; R6 together with R5 forms a -CH=CH-CH=CH- bridge; X2 is C-X6 or nitrogen; X1, X3 and X6 are independently hydrogen, halogen or trihalomethyl, wherein at least two of X1, X3 and X6 are not hydrogen; X4 is trifluoromethyl, difluoromethyl or chlorodifluoromethyl. The invention also provides intermediates useful for the preparation of compounds of formula (I), as well as methods of controlling insects, acarines, nematodes or molluscs using the compounds of formula (I).
    本发明提供了以下式(I)的化合物,其中G1为氧;R1为氢;R2为P基团;L为键,亚甲基或乙烯基;A1和A2中的一个为S,SO或SO2,另一个为-C(R4)R4;R3为氢或甲基;每个R4独立地为氢或甲基;Y1为C-R6,CH或氮;Y2和Y3独立地为CH或氮;其中Y1、Y2和Y3中不超过两个为氮,且Y2和Y3不同时为氮;R5为氢、卤素、氰基、硝基、NH2、C1-C2烷基、C1-C2卤代烷基、C3-C5环烷基、C3-C5卤代环烷基、C1-C2烷氧基、C1-C2卤代烷氧基;R6与R5一起形成-CH=CH-CH=CH-桥;X2为C-X6或氮;X1、X3和X6独立地为氢、卤素或三卤甲基,其中至少两个不是氢;X4为三氟甲基、二氟甲基或氯二氟甲基。该发明还提供了用于制备上述式(I)化合物的中间体,以及使用这些化合物控制昆虫、螨、线虫或软体动物的方法。
  • Ligand-controlled switch in diastereoselectivities: catalytic asymmetric construction of spirocyclic pyrrolidine-azetidine/oxe(thie)tane derivatives
    作者:Hua Deng、Renmeng Jia、Wu-Lin Yang、Xingxin Yu、Wei-Ping Deng
    DOI:10.1039/c9cc03589c
    日期:——
    An efficient catalytic asymmetric 1,3-dipolar cycloaddition of azomethine ylides with four-membered ring-containing exocyclic alkenes has been developed, and either the exo or endo spirocyclic pyrrolidine-azetidine/oxe(thie)tane derivatives were diastereodivergently generated by employing Cu(I)/tBu-Phosferrox and a Cu(I)/N,O–ligand complex, respectively. Notably, various heteroatom-containing (N, O
    已开发出一种有效的催化亚甲亚胺基化物与含四元环的环外烯烃的催化不对称1,3-偶极环加成反应,并且通过使用Cu()来非对映地生成exo或内螺环吡咯烷-氮杂环丁烷/ oxe(thie)tane衍生物。I)/ t Bu-Phosferrox和Cu(I)/ N,O-配体络合物。值得注意的是,发现各种含杂原子的(N,O,S)环外烯烃在该转化中具有良好的耐受性。
  • [EN] PYRIDAZINE DERIVATIVES AS RORC MODULATORS<br/>[FR] DÉRIVÉS DE PYRIDAZINE UTILISÉS EN TANT QUE MODULATEURS DE RORC
    申请人:HOFFMANN LA ROCHE
    公开号:WO2018083105A1
    公开(公告)日:2018-05-11
    Compounds of formula (I): (I) or pharmaceutical salts thereof, wherein m, n,, p, q A, B, Ri, R2, R3, R4, R5, R6and R7are as defined herein. Also disclosed are methods of making the compounds and using the compounds as RORs modulators for treatment of inflammatory diseases such as arthritis.
    式(I)的化合物或其药用盐,其中m、n、p、q、A、B、R1、R2、R3、R4、R5、R6和R7如本文所定义。还公开了制备这些化合物的方法,并将这些化合物用作RORs调节剂,用于治疗炎症性疾病,如关节炎。
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