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tert-butyl N-(4,5-dimethyl-1,3-thiazol-2-yl)carbamate | 1186298-91-8

中文名称
——
中文别名
——
英文名称
tert-butyl N-(4,5-dimethyl-1,3-thiazol-2-yl)carbamate
英文别名
——
tert-butyl N-(4,5-dimethyl-1,3-thiazol-2-yl)carbamate化学式
CAS
1186298-91-8
化学式
C10H16N2O2S
mdl
——
分子量
228.315
InChiKey
OUIXOWCUHGGCLC-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):
    2.7
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    79.5
  • 氢给体数:
    1
  • 氢受体数:
    4

文献信息

  • NOVEL 7-SUBSTITUTED 3-CARBOXY-OXADIAZINO-QUINOLONE DERIVATIVES, THEIR PREPARATION AND THEIR APPLICATION AS ANTI-BACTERIALS
    申请人:Ropp Sandrine
    公开号:US20090221565A1
    公开(公告)日:2009-09-03
    A subject of the invention is the compounds of formula (I): in which either R 1 represents H, OH, NH 2 , —(CH 2 ) m —NR a R b (m=0.1 or 2), R a and R b represent H, linear, branched or cyclic (C 1 -C 6 ) alkyl, (C 3 -C 6 ) cycloalkyl-(C 3 -C 6 )— alkyl, R c , S(O) 2 R c , C(O)R c , S(O) 2 R d or C(O)R d ; or R a and R b with N form an R c radical; R c represents a saturated, unsaturated or 5- or 6-members aromatic ring, containing 1 to 4 heteroatoms chosen from N, O and S, optionally substituted; R d represents a linear, branched or cyclic (C 1 -C 6 ) alkyl, optionally substituted by 1 to 4 halogens; or R 1 represents R c or CHR e R c or CHR e R d ; R e represents H, OH, NH 2 , NH—(C 1 -C 6 )-alk or N-(C 1 -C 6 )-alk 2 , or NH—(C 1 -C 7 )-acyl or NHR c ; R 2 represents H, (CH 2 ) m —NR a R b , R c , CHR e R c or CHR e R d , and R′ 2 represents H; it being understood that R 1 and R 2 cannot at the same time be H or that R 1 and R 2 or R 2 and R 1 cannot be one (CH 2 ) m —NR a R b or R c or H and the other one OH, or one H and the other one NH 2 , or one H and the other one (CH 2 ) m —NR a R b in which R a and R b represent H or alkyl or C(O)R d , in which R d represents an unsubstituted alkyl or cycloalkyl; or R 1 has the above definition except H and R 2 and R′ 2 together represent gem dialkyl or alkyl-oxime, or R 2 and R′ 2 represent respectively R c or R d and OH, NH 2 , NHR c or NHR f , R f being a (C 1 -C 7 ) acyl radical; or R 1 represents H and R 2 and R′ 2 together represent alkyl-oxime or one represents R c and the other one represents OH, NH 2 , NHR c or NHR f ; n is 0 or 1; R 3 and R′ 3 represent H or (C 1 -C 6 ) alkyl optionally substituted by 1 to 3 halogens or R 3 represents (C 1 -C 6 ) alkoxy carbonyl and R′ 3 represents H; R4 represents methyl optionally substituted by halogen; R 5 represents H, (C 1 -C 6 ) alkyl or (C 7 -C 12 ) arylalkyl; R 6 represents H, fluorine, NO 2 , CF 3 or CN; in the form of enantiomers or mixtures, as well as their salts with acids and bases; their preparation and their application as anti-bacterials, in both human and veterinary medicine.
    本发明的一个主题是化合物的公式(I):其中R1代表H、OH、NH2、—(CH2)m—NRaRb(m=0、1或2);Ra和Rb代表H、直链、支链或环状(C1-C6)烷基、(C3-C6)环烷基-(C3-C6)烷基、Rc、S(O)2Rc、C(O)Rc、S(O)2Rd或C(O)Rd;或Ra和Rb与N形成一个Rc基团;Rc代表饱和、不饱和或含有1至4个N、O和S中的杂原子的5-或6-成员芳香环,可选地取代;Rd代表直链、支链或环状(C1-C6)烷基,可选地取代1至4个卤素;或R1代表Rc或CHReRc或CHReRd;Re代表H、OH、NH2、NH—(C1-C6)-烷基或N-(C1-C6)-烷基2,或NH—(C1-C7)-酰基或NHRc;R2代表H、( )m—NRaRb、Rc、CHReRc或CHReRd,而R′2代表H;R1和R2不能同时为H,或者R1和R2或R2和R1不能一个为( )m—NRaRb或Rc或H,另一个为OH,或一个为H,另一个为NH2,或一个为H,另一个为( )m—NRaRb,其中Ra和Rb代表H或烷基或C(O)Rd,其中Rd代表未取代的烷基或环烷基;或R1具有上述定义,除了H,R2和R′2一起表示双取代烷基或烷基氧,或者R2和R′2分别表示Rc或Rd和OH、NH2、NHRc或NHRf,其中Rf是(C1-C7)酰基基团;或R1代表H,R2和R′2一起表示烷基氧,或一个表示Rc,另一个表示OH、NH2、NHRc或NHRf;n为0或1;R3和R′3表示H或可选地取代1至3个卤素的(C1-C6)烷基,或R3表示(C1-C6)烷氧羰基,R′3表示H;R4表示可选地取代的甲基;R5表示H、(C1-C6)烷基或(C7-C12)芳基烷基;R6表示H、NO2CF3或CN;以对映体或混合物形式存在,以及它们与酸和碱形成的盐;它们的制备以及它们作为抗菌剂在人类和兽医学中的应用。
  • NOVEL TRIAZINE COMPOUNDS
    申请人:Dugar Sundeep
    公开号:US20130303516A1
    公开(公告)日:2013-11-14
    The present invention relates to novel triazine compounds of formula (1), methods of their preparation, pharmaceutical compositions containing these compounds and the use of these compounds to treat proliferative disorders such as tumors and cancers and also other conditions and disorders related to or associated with dysregulation of PI3 Kinases, PI3 Kinase pathway, mTOR and/or the mTOR pathway.
    本发明涉及公式(1)的新型三嗪类化合物,其制备方法、含有这些化合物的药物组合物以及使用这些化合物治疗增殖性疾病,如肿瘤和癌症,以及与PI3激酶、PI3激酶途径、mTOR和/或mTOR途径失调相关或相关的其他状况和疾病。
  • US7713965B2
    申请人:——
    公开号:US7713965B2
    公开(公告)日:2010-05-11
  • US9481670B2
    申请人:——
    公开号:US9481670B2
    公开(公告)日:2016-11-01
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