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

3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate

中文名称
——
中文别名
——
英文名称
3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate
英文别名
3,3-Dioxido-1,3-benzoxathiol-6-yl trifluoromethanesulfonate;(3,3-dioxo-1,3λ6-benzoxathiol-6-yl) trifluoromethanesulfonate
3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate化学式
CAS
——
化学式
C8H5F3O6S2
mdl
MFCD28897440
分子量
318.251
InChiKey
OZUCBBKUHJAOHP-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):
    1.8
  • 重原子数:
    19
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    104
  • 氢给体数:
    0
  • 氢受体数:
    9

反应信息

  • 作为反应物:
    描述:
    3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate(1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride偶氮二甲酸二异丙酯三苯基膦 作用下, 以 四氢呋喃甲苯 为溶剂, 反应 27.0h, 生成 tert-butyl 4-(5-((4-(3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl)-2-fluorophenoxy)methyl)thiazol-2-yl)piperidine-1-carboxylate
    参考文献:
    名称:
    [EN] COMPOUNDS CONTAINING POLYSUBSTITUTED BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXIDE OR BENZO[D][1,3]OXATHIOLE 3,3-DIOXIDE AND METHODS/USES THEREOF AS AGONISTS OF G PROTEIN-COUPLED RECEPTOR 119
    [FR] COMPOSÉS CONTENANT DU BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXYDE OU DU BENZO[D][1,3]OXATHIOLE 3,3-DIOXYDE POLYSUBSTITUÉ, ET LEURS PROCÉDÉS/UTILISATIONS EN TANT QU'AGONISTES DU RÉCEPTEUR 119 COUPLÉ À LA PROTÉINE G
    摘要:
    提供具有化学式(I)的化合物,其中:X1和X2从O、S、SO和SO2的某些组合中选择;X3从CH、CF和N中选择;X4从CH和N中选择;X6、X6'和X6''从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基和酰胺基中选择;X7和X7'从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基、氨基烷基和酰胺基中选择,或者X7和X7'一起形成环烷基或杂环;A从某些可选择取代的烷氧基、哌嗪基和吡咯烷基中选择。还提供包含这些化合物的组合物,以及与之相关的用途/方法,包括治疗与GPR119失调、2型糖尿病以及相关代谢紊乱相关的疾病和症状。
    公开号:
    WO2019104418A1
  • 作为产物:
    描述:
    噻克索酮吡啶18-冠醚-6 、 palladium 10% on activated carbon 、 氢气双氧水potassium carbonate溶剂黄146 作用下, 以 四氢呋喃乙腈 为溶剂, 反应 48.0h, 生成 3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate
    参考文献:
    名称:
    [EN] COMPOUNDS CONTAINING POLYSUBSTITUTED BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXIDE OR BENZO[D][1,3]OXATHIOLE 3,3-DIOXIDE AND METHODS/USES THEREOF AS AGONISTS OF G PROTEIN-COUPLED RECEPTOR 119
    [FR] COMPOSÉS CONTENANT DU BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXYDE OU DU BENZO[D][1,3]OXATHIOLE 3,3-DIOXYDE POLYSUBSTITUÉ, ET LEURS PROCÉDÉS/UTILISATIONS EN TANT QU'AGONISTES DU RÉCEPTEUR 119 COUPLÉ À LA PROTÉINE G
    摘要:
    提供具有化学式(I)的化合物,其中:X1和X2从O、S、SO和SO2的某些组合中选择;X3从CH、CF和N中选择;X4从CH和N中选择;X6、X6'和X6''从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基和酰胺基中选择;X7和X7'从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基、氨基烷基和酰胺基中选择,或者X7和X7'一起形成环烷基或杂环;A从某些可选择取代的烷氧基、哌嗪基和吡咯烷基中选择。还提供包含这些化合物的组合物,以及与之相关的用途/方法,包括治疗与GPR119失调、2型糖尿病以及相关代谢紊乱相关的疾病和症状。
    公开号:
    WO2019104418A1
点击查看最新优质反应信息

文献信息

  • [EN] COMPOUNDS CONTAINING POLYSUBSTITUTED BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXIDE OR BENZO[D][1,3]OXATHIOLE 3,3-DIOXIDE AND METHODS/USES THEREOF AS AGONISTS OF G PROTEIN-COUPLED RECEPTOR 119<br/>[FR] COMPOSÉS CONTENANT DU BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXYDE OU DU BENZO[D][1,3]OXATHIOLE 3,3-DIOXYDE POLYSUBSTITUÉ, ET LEURS PROCÉDÉS/UTILISATIONS EN TANT QU'AGONISTES DU RÉCEPTEUR 119 COUPLÉ À LA PROTÉINE G
    申请人:PRAMANA PHARMACEUTICALS INC
    公开号:WO2019104418A1
    公开(公告)日:2019-06-06
    There are provided compounds having formula (I), in which: X1 and X2 are selected from certain combinations of O, S, SO and SO2; X3 is selected from CH, CF and N; X4 is selected from CH and N; X6, X6' and X6'' are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, and amide groups; X7 and X7' are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, aminoalkyl and amide groups, or both X7 and X7' together form a cycloalkyl or heterocycle; and A is selected from certain optionally substituted, alkoxy, piperazinyl and pyrrolidinyl groups. Also provided are compositions comprising these compounds, as well as uses/methods related thereto, including treatment of diseases and conditions associated with GPR119 dysregulation, Type 2 diabetes mellitus, and related metabolic disorders. (I)
    提供具有化学式(I)的化合物,其中:X1和X2从O、S、SO和SO2的某些组合中选择;X3从CH、CF和N中选择;X4从CH和N中选择;X6、X6'和X6''从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基和酰胺基中选择;X7和X7'从H、卤素以及某些烷基、卤代烷基、烷氧基、羟基烷基、氨基烷基和酰胺基中选择,或者X7和X7'一起形成环烷基或杂环;A从某些可选择取代的烷氧基、哌嗪基和吡咯烷基中选择。还提供包含这些化合物的组合物,以及与之相关的用途/方法,包括治疗与GPR119失调、2型糖尿病以及相关代谢紊乱相关的疾病和症状。
  • Compounds containing benzo[d][1,3]oxathiole, benzo[d][1,3]oxathiole 3-oxide or benzo[d][1,3]oxathiole 3,3-dioxide and methods/uses thereof as agonists of g protein-coupled receptor 119
    申请人:PRAMANA PHARMACEUTICALS INC.
    公开号:US10906894B2
    公开(公告)日:2021-02-02
    There are provided compounds containing benzo[d][1,3]oxathiole, benzo[d][1,3]oxathiole 3-oxide, and benzo[d][1,3]oxathiole 3,3-dioxide, as well as uses/methods related thereto, including treatment of diseases and condition associated with GPR119 dysregulation, Type 2 diabetes mellitus, and related metabolic disorders.
    提供了含有苯并[d][1,3]氧硫杂环戊烯、苯并[d][1,3]氧硫杂环戊烯 3-氧化物和苯并[d][1,3]氧硫杂环戊烯 3,3- 二氧化物的化合物,以及与之相关的用途/方法,包括治疗与 GPR119 失调、2 型糖尿病和相关代谢紊乱有关的疾病和病症。
  • Compounds containing polysubstituted benzo[d][1,3]oxathiole, benzo[d][1,3]oxathiole 3-oxide or benzo[d][1,3]oxathiole 3,3-dioxide and methods/uses thereof as agonists of G protein-coupled receptor 119
    申请人:PRAMANA PHARMACEUTICALS INC.
    公开号:US11358956B2
    公开(公告)日:2022-06-14
    There are provided compounds having formula (I), in which: X1 and X2 are selected from certain combinations of O, S, SO and SO2; X3 is selected from CH, CF and N; X4 is selected from CH and N; X6, X6′ and X6″ are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, and amide groups; X7 and X7′ are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, aminoalkyl and amide groups, or both X7 and X7′ together form a cycloalkyl or heterocycle; and A is selected from certain optionally substituted, alkoxy, piperazinyl and pyrrolidinyl groups. Also provided are compositions comprising these compounds, as well as uses/methods related thereto, including treatment of diseases and conditions associated with GPR119 dysregulation, Type 2 diabetes mellitus, and related metabolic disorders. (I)
    提供了具有式(I)的化合物,其中:X1和X2选自O、S、SO和SO2的某些组合;X3选自CH、CF和N;X4选自CH和N;X6、X6′和X6″选自H、卤素和某些烷基、卤代烷基、烷氧基、羟基烷基和酰胺基团;X7和X7′选自H、卤素和某些烷基、卤代烷基、烷氧基、羟基烷基、氨基烷基和酰胺基团,或X7和X7′共同形成环烷基或杂环;A选自某些任选取代的烷氧基、哌嗪基和吡咯烷基团。还提供了包含这些化合物的组合物,以及与之相关的用途/方法,包括治疗与 GPR119 失调、2 型糖尿病和相关代谢紊乱有关的疾病和病症。(I)
  • COMPOUNDS CONTAINING BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXIDE OR BENZO[D][1,3]OXATHIOLE 3,3-DIOXIDE AND METHODS/USES THEREOF AS AGONISTS OF G PROTEIN-COUPLED RECEPTOR 119
    申请人:PRAMANA PHARMACEUTICALS INC.
    公开号:US20190292173A1
    公开(公告)日:2019-09-26
    There are provided compounds containing benzo[d][1,3]oxathiole, benzo[d][1,3]oxathiole 3-oxide, and benzo[d][1,3]oxathiole 3,3-dioxide, as well as uses/methods related thereto, including treatment of diseases and condition associated with GPR119 dysregulation, Type 2 diabetes mellitus, and related metabolic disorders.
  • COMPOUNDS CONTAINING POLYSUBSTITUTED BENZO[D][1,3]OXATHIOLE, BENZO[D][1,3]OXATHIOLE 3-OXIDE OR BENZO[D][1,3]OXATHIOLE 3,3-DIOXIDE AND METHODS/USES THEREOF AS AGONISTS OF G PROTEIN-COUPLED RECEPTOR 119
    申请人:PRAMANA PHARMACEUTICALS INC.
    公开号:US20210188825A1
    公开(公告)日:2021-06-24
    There are provided compounds having formula (I), in which: X 1 and X 2 are selected from certain combinations of O, S, SO and SO 2 ; X 3 is selected from CH, CF and N; X 4 is selected from CH and N; X 6 , X 6′ and X 6″ are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, and amide groups; X 7 and X 7′ are selected from H, halogen, and certain alkyl, haloalkyl, alkoxy, hydroxyalkyl, aminoalkyl and amide groups, or both X 7 and X 7′ together form a cycloalkyl or heterocycle; and A is selected from certain optionally substituted, alkoxy, piperazinyl and pyrrolidinyl groups. Also provided are compositions comprising these compounds, as well as uses/methods related thereto, including treatment of diseases and conditions associated with GPR119 dysregulation, Type 2 diabetes mellitus, and related metabolic disorders. (I)
查看更多

同类化合物

四碘-2-磺基苯酸酐 四溴-2-磺基苯甲酸环酐 N,N'-二[[(1,3-苯并氧硫杂环戊烷-2-基)硫代]甲基]脲 5-羟基-4,6,7-三甲基-2-丙基-1,3-苯并氧杂噻唑 3-(5-羟基-4,6,7-三甲基-1,3-苯并氧杂噻唑-2-基)丙醇 2-磺基苯甲酸酐 2-(2-甲氧基丙烷-2-基)-7,7-二甲基-4-叔-丁基-8-氧杂-9-硫杂双环[4.3.0]壬-2,4,10-三烯 1,3-苯并噁噻唑,5-甲氧基-,3,3-二氧化 5,7-dimethyl-2-(2,2,2-trifluoro-1-methoxycarbonylethylidene)-1,3-benzooxathiole trans-6-fluoro-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide cis-6-fluoro-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide trans-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide cis-2',5-dimethoxy-6'-(trifluoromethyl)spiro[1,3-benzoxathiole-2,1'-cyclohex-2'-en]-4'-one 3,3-dioxide (2R,SS)-2-[(1S)-1-(4-methylphenyl)-1-(4-methoxyphenylamino)-methyl]-1,3-benzoxathiole 3(2H)-oxide 3,3-bis<(4-dimethylamino)phenyl>-4H-2,1-benzoxathiole 1-oxide 6-methyl-3,3-bis(4-dimethylaminophenyl)-3H-2,1-benzoxathiole 1-oxide (S)-6-(4-((R)-1-(5-ethylpyrimidin-2-yl)pyrrolidin-3-yl)methoxy-3-fluorophenyl)-2H-benzo[d][1,3]oxathiole 3-oxide 1,3-benzoxathiol-6-ol 1,3-benzoxathiol-6-ol-3-oxide 3,3-dioxido-2H-benzo[d][1,3]oxathiol-6-yl trifluoromethanesulfonate 5-(5-t-butyldimethylsilyloxy-4,6,7-trimethyl-1,3-benzoxathiole-2-yl)-2,2-dimethylpentanoic acid trans-6-fluoro-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide cis-6-fluoro-2',5-dimethoxy-6'-methylspiro(1,3-benzoxathiole-2,1'-cyclohex-2'-en)-4'-one 3,3-dioxide spiro<1,3-benzoxathiole-2,1'-cyclohexane> 3-oxide 4-Amino-3,3-dioxo-3λ6-benz[1,3]oxathiol-5-ol 6-Fluoro-1,3-benzoxathiol-2-amine 3H-2,1-Benzoxathiole 1,3-Benzoxathiole, 5-(1-(2-(2-ethoxyethoxy)ethoxy)ethoxy)- 4-[2-(4-Chloro-phenyl)-benzo[1,3]dithiol-2-yl]-2-[2-(4-chloro-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 5-hydroxy-1,3-benzoxathiole 1,3-Benzoxathiole, 5-(1-(2-(4-chlorophenoxy)ethoxy)ethoxy)- 4-[2-(4-Methoxy-phenyl)-benzo[1,3]dithiol-2-yl]-2-[2-(4-methoxy-phenyl)-benzo[1,3]oxathiol-2-yl]-1H-pyrrole 5-hydroxy-2H-benzo[d][1,3]oxathiole 3,3-dioxide 4-(2-Methyl-benzo[1,3]dithiol-2-yl)-2-(2-methyl-benzo[1,3]oxathiol-2-yl)-1H-pyrrole 2,5-bis<2-(2-tert-butyl-1,3-benzoxathiolyl)>pyrrole 5-bromo-2-phenylbenzo[d][1,3]oxathiole 5-hydroxy-4,6,7-trimethyl-1,3-benzoxathiole 5-Ethoxy-1,1-dioxo-1H-1λ6-benzo[c][1,2]oxathiol-3-one 5-Butoxy-1,1-dioxo-1H-1λ6-benzo[c][1,2]oxathiol-3-one 2-t-Butyl-1,3-benzoxathiole 2-methyl-5'-nitrospiro(3H-2,1-benzoxathiole-1,1'-3H-1,2-benzisothiazole)-3(2H),3'-dione 2,5'-dimethylspiro(3H-2,1-benzoxathiole-1,1'-3H-1,2-benzisothiazole)-3(2H),3'-dione 3,3,3',3'-tetrakis(trifluoromethyl)-1,1'-spirobi<3H-2,1-benzoxathiole> 1-oxide 3-imino-3H-2,1-benzoxathiole-1,1-dioxide Bis-(2-carboxyphenyl)-Schwefel-dihydroxid-dilacton 6-tert-Butyl-1,1,2a,4,4-pentamethyl-2a,4-dihydro-1H-2,3-dioxa-2aλ4-thia-cyclopenta[cd]indene 2,2-dimethyl-6-oxo-8-phenyl-2H,6H-<1,2>thioxolo<4,5,1-hi>benzthioxole 2-(5-Tert-butyl-3,3-dimethyl-2,1-benzoxathiol-7-yl)propan-2-ol 9-tert-Butyl-2,2,4,6,6-pentamethyl-3,5-dioxa-4λ4-thia-tricyclo[5.3.1.04,11]undeca-1(10),7(11),8-triene 4-oxide 2-(5-tert-Butyl-1-chloro-1,3,3-trimethyl-1,3-dihydro-1λ4-benzo[c][1,2]oxathiol-7-yl)-propan-2-ol