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

2-amino-6-difluoromethoxy-benzonitrile | 1174315-56-0

中文名称
——
中文别名
——
英文名称
2-amino-6-difluoromethoxy-benzonitrile
英文别名
2-amino-6-(difluoromethoxy)benzonitrile
2-amino-6-difluoromethoxy-benzonitrile化学式
CAS
1174315-56-0
化学式
C8H6F2N2O
mdl
——
分子量
184.145
InChiKey
YSSZPLSMFYIQJG-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:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.12
  • 拓扑面积:
    59
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • [EN] SULFOXIMINE SUBSTITUTED QUINAZOLINES FOR PHARMACEUTICAL COMPOSITIONS<br/>[FR] QUINAZOLINES SUBSTITUÉES PAR UNE SULFOXIMINE DESTINÉES À DES COMPOSITIONS PHARMACEUTIQUES
    申请人:BOEHRINGER INGELHEIM INT
    公开号:WO2015082324A1
    公开(公告)日:2015-06-11
    This invention relates to novel sulfoximine substituted quinazoline derivatives of formula (I), wherein Ar, R1 and R2 are as defined in the description and claims, and their use as MNK1 (MNK1a or MNK1b) and/or MNK2 (MNK2a or MNK2b) kinase inhibitors, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment or amelioration of MNK1 (MNK1a or MNK1b) and/or MNK2 (MNK2a or MNK2b) mediated disorders.
    这项发明涉及一种新型的磺酰胺取代的喹唑啉衍生物,其化学式为(I),其中Ar、R1和R2如描述和索赔中定义,以及它们作为MNK1(MNK1a或MNK1b)和/或MNK2(MNK2a或MNK2b)激酶抑制剂的用途,含有这些化合物的药物组合物,以及将其用作治疗或改善MNK1(MNK1a或MNK1b)和/或MNK2(MNK2a或MNK2b)介导的疾病的药物的方法。
  • Chemical compounds
    申请人:Maienfisch Peter
    公开号:US08524896B2
    公开(公告)日:2013-09-03
    A compound of the formula (I) where, for example, W, X and Y are each CH; R1 and R6 together with the adjacent nitrogen forms a 3 to 10-membered saturated ring, wherein the ring may contain, in addition to the nitrogen and carbon ring members, 1, 2 or 3 heteroatoms and/or heteroatom groups as ring members, independently of one another, selected from the group consisting of sulfur, CO, SO, SO2 and N—R7 and/or the ring may carry 1, 2 or 3 radicals, independently of one another, each selected, for example, from the group consisting of halogen, cyano, nitro, amino, and C1-C6-alkyl. R2 is, for example, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy or C1-C6-alkoxy-C1-C6-alkoxy, and R7 is for example, R10C(═O), C1-C6 alkyl or C1-C6-haloalkyl; and/or salts thereof; and their use as pesticidal agents.
    化合物的式子(I),其中,例如,W、X和Y均为CH;R1和R6与相邻的氮形成一个3到10个成员的饱和环,其中该环可以包含除氮和碳环成员之外的1、2或3个杂原子和/或杂原子基作为环成员,独立于彼此,从所述群组中选出,所述群组由硫、CO、SO、SO2和N-R7组成,和/或该环可以携带1、2或3个基团,独立于彼此,每个基团例如从卤素、氰基、硝基、氨基和C1-C6烷基中选出。例如,R2是卤素、C1-C6烷基、C1-C6卤代烷基、C1-C6烷氧基、C1-C6卤代烷氧基或C1-C6-烷氧基-C1-C6-烷氧基,R7例如为R10C(═O)、C1-C6烷基或C1-C6卤代烷基;以及它们的盐;以及它们作为杀虫剂的用途。
  • CHEMICAL COMPOUNDS
    申请人:Pitterna Thomas
    公开号:US20100311582A1
    公开(公告)日:2010-12-09
    A compound of the formula (I) where, for example, W, X and Y are each CH; R 1 and R 6 , independently of each other, are for example, selected from the group consisting of H, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy, C3-C8-cycloalkyl, R 7 C(═O), and a ring system; provided that at least one of R 1 and R 6 is a —C2-C6-alkenylthio-C1-C6-alkyl, —C1-C6-alkoxy-C(═O)NRx-C1-C6-alkyl, —partially or fully unsaturated ring system containing in at least one ring in the ring system at least one hetero atom selected from N, O and S, which ring system is bound (i.e. through the N bonded to R 1 and R 6 in formula I) either directly or via a a C1-C6-alkylene group to the remainder of the compound, —partially or fully unsaturated ring system containing a ring that is bound to the remainder of the compound (i.e. through the N bonded to R 1 and R 6 in formula I) via a C1-C6-alkylene group, which group contains at least one hetero atom and/or heteroatom group selected from N, O, S, SO, SO 2 , and C(=0), —a ring system having a 5- to 14-membered bicylic ring which may be unsubstituted or be substituted with 1, 2 or 3, independently of one another, radicals selected from halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy and C1-C6-haloalkoxy, or —(C3-C8-cyloalkyl)thio-C1-C6-alkyl; R 2 is, for example, H, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy or C1-C6-alkoxy-C1-C6-alkoxy, and/or salts thereof; and their use as pesticidal agents.
    化合物的公式(I),其中,例如,W、X和Y都是CH;R1和R6彼此独立,例如,从H、C1-C6-烷基、C2-C6-烯基、C2-C6-炔基、C1-C6-烷氧基、C3-C8-环烷基、R7C(═O)和环系组成的群中选择;前提是R1和R6中至少有一个是-C2-C6-烯基硫基-C1-C6-烷基,-C1-C6-烷氧基-C(═O)NRx-C1-C6-烷基,部分或完全不饱和的环系,其中在环系中至少有一个环中含有N、O和S中选择的至少一个杂原子,该环系通过式I中与R1和R6结合的N直接或通过C1-C6-烷基链与化合物的其余部分结合,部分或完全不饱和的环系,其中有一个环通过C1-C6-烷基链与化合物的其余部分结合,该链含有至少一个N、O、S、SO、SO2和C(=0)中选择的杂原子和/或杂原子基,具有5-至14-成员的双环环系,可以是未取代的或被1、2或3个彼此独立的基团(选择自卤素、C1-C6-烷基、C1-C6-卤代烷基、C1-C6-烷氧基和C1-C6-卤代烷氧基)取代的;R2,例如,是H、卤素、C1-C6-烷基、C1-C6-卤代烷基、C1-C6-烷氧基、C1-C6-卤代烷氧基或C1-C6-烷氧基-C1-C6-烷氧基,和/或其盐;以及它们作为杀虫剂的用途。
  • 2-Cyanophenyl Sulfonamide Derivatives Useful as Pesticides
    申请人:Syngenta Participations AG
    公开号:EP2500340A1
    公开(公告)日:2012-09-19
    A compound of the formula I where, for example, W, X and Y are each CH; R1 and R6, independently of each other, are for example, selected from the group consisting of H, C1-C6-alkyl, C2-C6-alkenyl, C2-C6-alkynyl, C1-C6-alkoxy, C3-C8-cycloalkyl, R7C(=O), and a ring system; provided that at least one of R1 and R6 is a - partially or fully unsaturated ring system containing in at least one ring in the ring system at least one hetero atom selected from N, O and S, which ring system is bound (i.e. through the N bonded to R1 and R6 in formula I) either directly or via a a C1-C6-alkylene group to the remainder of the compound, - a ring system having a 5- to 14-membered bicylic ring which may be unsubstituted or be substituted with 1, 2 or 3, independently of one another, radicals selected from halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy and C1-C6-haloalkoxy, or R2 is, for example,H, halogen, C1-C6-alkyl, C1-C6-haloalkyl, C1-C6-alkoxy, C1-C6-haloalkoxy or C1-C6-alkoxy-C1-C6-alkoxy, and/or salts thereof; and their use as as pesticidal agents.
    式 I 的化合物 其中,W、X 和 Y 各为 CH; R1 和 R6 相互独立,例如选自由 H、C1-C6-烷基、C2-C6-烯基、C2-C6-炔基、C1-C6-烷氧基、C3-C8-环烷基、R7C(=O) 和环系统组成的组; 条件是 R1 和 R6 中至少有一个是 - 部分或完全不饱和环系,在环系的至少一个环中含有至少一个选自 N、O 和 S 的杂原子,该环系直接或通过一个 C1-C6- 烷基与化合物的其余部分结合(即通过式 I 中与 R1 和 R6 结合的 N)、 - 具有 5 至 14 元双环的环系,该环系可以未被取代,也可以被 1、2 或 3 个彼此独立的基取代,这些基选自卤素、C1-C6-烷基、C1-C6-卤代烷基、C1-C6-烷氧基和 C1-C6-卤代烷氧基,或 R2 例如是 H、卤素、C1-C6-烷基、C1-C6-卤代烷基、C1-C6-烷氧基、C1-C6-卤代烷氧基或 C1-C6- 烷氧基-C1-C6-烷氧基、 和/或其盐类;以及它们作为杀虫剂的用途。
  • Sulfoximine substituted quinazolines for pharmaceutical compositions
    申请人:EVOTEC INTERNATIONAL GMBH
    公开号:US10093660B2
    公开(公告)日:2018-10-09
    This invention relates to novel sulfoximine substituted quinazoline derivatives of formula (I), wherein Ar, R1 and R2 are as defined in the description and claims, and their use as MNK1 (MNK1a or MNK1b) and/or MNK2 (MNK2a or MNK2b) kinase inhibitors, pharmaceutical compositions containing the same, and methods of using the same as agents for treatment or amelioration of MNK1 (MNK1a or MNK1b) and/or MNK2 (MNK2a or MNK2b) mediated disorders.
    本发明涉及式(I)的新型硫代亚胺取代的喹唑啉衍生物,其中Ar、R1和R2如说明书和权利要求书中所定义,以及它们作为MNK1(MNK1a或MNK1b)和/或MNK2(MNK2a或MNK2b)激酶抑制剂的用途、含有这些物质的药物组合物,以及将这些物质用作治疗或改善 MNK1(MNK1a 或 MNK1b)和/或 MNK2(MNK2a 或 MNK2b)介导的疾病的药物的方法。
查看更多