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1,1-二氧化物-3-氨基硫杂环丁烷 | 88511-13-1

中文名称
1,1-二氧化物-3-氨基硫杂环丁烷
中文别名
——
英文名称
1,1-dioxothietan-3-amine
英文别名
3-aminothietane 1,1-dioxide
1,1-二氧化物-3-氨基硫杂环丁烷化学式
CAS
88511-13-1
化学式
C3H7NO2S
mdl
MFCD18445741
分子量
121.16
InChiKey
QYOJSNPPGRBNJR-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):
    -1.5
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    68.5
  • 氢给体数:
    1
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    1,1-二氧化物-3-氨基硫杂环丁烷 、 4-[5-(3,5-dichlorophenyl)-5-trifluoromethyl-4,5-dihydroisoxazol-3-yl]-2-fluoro benzoic acid 在 双(2-氧代-3-恶唑烷基)次磷酰氯N,N-二异丙基乙胺 作用下, 以 N,N-二甲基乙酰胺 为溶剂, 反应 16.0h, 生成 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4H-1,2-oxazol-3-yl]-N-(1,1-dioxothietan-3-yl)-2-fluorobenzamide
    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
  • 作为产物:
    参考文献:
    名称:
    Diggle, Andrew W.; Griffiths, Gwerydd; Young, David J., Bulletin de la Societe Chimique de France, 1988, # 2, p. 317 - 321
    摘要:
    DOI:
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文献信息

  • [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:WO2013026726A1
    公开(公告)日:2013-02-28
    The present invention provides compounds of formula I wherein Q is Q1 or Q2; A1, A2, A3 and A4 are independently of each other C-H, C-R7, or nitrogen; R1 is C1-C8haloalkyl; R2 is aryl or aryl substituted by one to five R11, or heteroaryl or heteroaryl substituted by one to five R11; and R3, R4, R5, R6 and R7 are as defined in the claims. The invention also provides methods of controlling insects, acarines, nematodes or molluscs which methods comprise applying to a pest, to a locus of a pest, or to a plant susceptible to attack by a pest an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula (I).
    本发明提供了式I的化合物,其中Q是Q1或Q2;A1、A2、A3和A4分别独立地为C-H、C-R7或氮;R1为C1-C8卤代烷基;R2为芳基或被1至5个R11取代的芳基,或者为杂环芳基或被1至5个R11取代的杂环芳基;以及R3、R4、R5、R6和R7如权利要求中所定义的。该发明还提供了控制昆虫、螨虫、线虫或软体动物的方法,该方法包括向害虫、害虫的生境或易受害虫侵害的植物施加式(I)的化合物的杀虫、杀螨、杀线虫或杀软体动物的有效量。
  • [EN] SUBSTITUTED PYRROLO TRIAZINE CARBOXAMIDE DERIVATIVES AS PROSTAGLANDIN EP3 RECEPTOR ANTAGONISTS<br/>[FR] DÉRIVÉS DE PYRROLO TRIAZINE CARBOXAMIDE SUBSTITUÉS EN TANT QU'ANTAGONISTES DU RÉCEPTEUR DE LA PROSTAGLANDINE EP3
    申请人:BAYER AG
    公开号:WO2021094209A1
    公开(公告)日:2021-05-20
    The invention relates to substituted pyrrole triazine carboxamide derivatives of formula (I) and to processes for their preparation, and also /to their use for preparing medicaments for the treatment and/ or prophylaxis of diseases, in particular cardiovascular disorders, preferably thrombotic or thromboembolic disorders, and diabetes, and also urogenital and ophthalmic disorders.
    这项发明涉及式(I)的取代吡咯三嗪羧酰胺衍生物,以及它们的制备方法,还有用于制备治疗和/或预防疾病的药物,特别是心血管疾病,优选为血栓性或血栓栓塞性疾病,糖尿病,以及泌尿生殖和眼科疾病。
  • 6-AMINOPYRIDIN-3-YL THIAZOLES AS MODULATORS OF RORyT
    申请人:Janssen Pharmaceutica NV
    公开号:US20170313691A1
    公开(公告)日:2017-11-02
    The present invention comprises compounds of Formula I. wherein: A 1 , A 2 , A 3 , A 4 , A 5 , R 1 , and R 2 are defined in the specification. The invention also comprises a method of treating or ameliorating a syndrome, disorder or disease, wherein the syndrome, disorder or disease is rheumatoid arthritis or psoriasis. The invention also comprises a method of modulating RORγt activity in a mammal by administration of a therapeutically effective amount of at least one compound of Formula I.
    本发明涵盖了Formula I的化合物。 其中: A1,A2,A3,A4,A5,R1和R2在说明书中有定义。 该发明还涵盖了一种治疗或改善综合症、疾病或疾病的方法,其中该综合症、疾病为类风湿性关节炎或牛皮癣。该发明还涵盖了通过给哺乳动物施用Formula I中至少一种化合物的治疗有效量来调节RORγt活性的方法。
  • [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。
  • [EN] INSECTICIDAL COMPOUNDS<br/>[FR] COMPOSÉS INSECTICIDES
    申请人:SYNGENTA PARTICIPATIONS AG
    公开号:WO2012126881A1
    公开(公告)日:2012-09-27
    The present invention relates to novel triazole derivatives of formula (I) having insecticidal activity, to processes and intermediates for preparing them, to insecticidal, acaricidal, nematicidal or molluscicidal compositions comprising them and to methods of using them to combat and control insect, acarine, nematode or mollusc pests wherein A1, A2, A3, A4, A5, A6, G1, G2, R1, R2, R3, L, Q1, Q2, R4, R5, R6, R7, Q2, Y1, Y2, Y3, Y4, Y5, Y6, Y7, Y8, and Y9 are as defined in claim 1; or salts or N-oxides thereof.
    本发明涉及具有杀虫活性的新型三唑衍生物(I)的公式,涉及制备它们的过程和中间体,涉及包含它们的杀虫剂、杀螨剂、杀线虫剂或杀软体动物剂的组合物,以及使用它们来对抗和控制昆虫、螨虫、线虫或软体动物害虫的方法,其中A1、A2、A3、A4、A5、A6、G1、G2、R1、R2、R3、L、Q1、Q2、R4、R5、R6、R7、Q2、Y1、Y2、Y3、Y4、Y5、Y6、Y7、Y8和Y9如权利要求1所定义;或其盐或N-氧化物。
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