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(-)-N-[[(5S)-3-(3,4-dihydro-1H-2-benzothiopyran-7-yl)-2-oxo-5-oxazolidinyl]methyl]acetamide | 444587-52-4

中文名称
——
中文别名
——
英文名称
(-)-N-[[(5S)-3-(3,4-dihydro-1H-2-benzothiopyran-7-yl)-2-oxo-5-oxazolidinyl]methyl]acetamide
英文别名
N-[[(5S)-3-(3,4-dihydro-1H-isothiochromen-7-yl)-2-oxo-1,3-oxazolidin-5-yl]methyl]acetamide
(-)-N-[[(5S)-3-(3,4-dihydro-1H-2-benzothiopyran-7-yl)-2-oxo-5-oxazolidinyl]methyl]acetamide化学式
CAS
444587-52-4
化学式
C15H18N2O3S
mdl
——
分子量
306.386
InChiKey
PVXSNCQIBMDSSJ-AWEZNQCLSA-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):
    1.3
  • 重原子数:
    21
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.47
  • 拓扑面积:
    83.9
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    (-)-N-[[(5S)-3-(3,4-dihydro-1H-2-benzothiopyran-7-yl)-2-oxo-5-oxazolidinyl]methyl]acetamide甲醇乙醚 为溶剂, 以72%的产率得到(+)-N-[[(5S)-3-(3,4-dihydro-1H-2-benzothiopyran-7-yl)-2-oxo-5-oxazolidinyl]methyl]ethanethioamide
    参考文献:
    名称:
    Oxazolidinones having a benzannulated 6- or 7-membered heterocycle
    摘要:
    本发明提供了具有苯并环的6-或7-员杂环的噁唑烷酮类作为抗菌剂。
    公开号:
    US20020133021A1
  • 作为产物:
    描述:
    phenylmethyl (3,4-dihydro-1H-2-benzothiopyran-7-yl)carbamate 以70%的产率得到(-)-N-[[(5S)-3-(3,4-dihydro-1H-2-benzothiopyran-7-yl)-2-oxo-5-oxazolidinyl]methyl]acetamide
    参考文献:
    名称:
    Oxazolidinones having a benzannulated 6- or 7-membered heterocycle
    摘要:
    本发明提供了具有苯并环的6-或7-员杂环的噁唑烷酮类作为抗菌剂。
    公开号:
    US20020133021A1
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文献信息

  • Amide-containing compound having improved solubility and method of improving the solubility of an amide-containing compound
    申请人:——
    公开号:US20040014967A1
    公开(公告)日:2004-01-22
    The present invention is directed to novel amide-containing compounds which have an improved solubility and a method of improving the solubility of amide-containing compounds. The amide-containing compounds include oxazolidinone compounds and the bioavailability of these oxazolidinone compounds is improved by improving the solubility thereof.
    本发明涉及具有改善溶解性的新型酰胺化合物,以及改善酰胺化合物溶解性的方法。这些酰胺化合物包括噁唑烷酮化合物,通过改善其溶解性来提高这些噁唑烷酮化合物的生物利用度。
  • Oxazolidinones having a benzannulated 6- or 7-membered heterocycle
    申请人:Johnson Paul D.
    公开号:US06972286B2
    公开(公告)日:2005-12-06
    The present invention provides oxazolidinones having a benzannelated 6- or 7-membered heterocycle as antibacterial agents.
    本发明提供了带有苯并6-或7-成员杂环的噁唑烷类化合物作为抗菌剂。
  • OXAZOLIDINONES HAVING A BENZANNULATED 6-OR 7-MEMBERED HETEROCYCLE AS ANTIBACTERIAL AGENTS
    申请人:Pharmacia & Upjohn Company
    公开号:EP1337530A1
    公开(公告)日:2003-08-27
  • AMIDE DERIVATIVES HAVING IMPROVED SOLUBILITY
    申请人:PHARMACIA & UPJOHN COMPANY
    公开号:EP1451164A2
    公开(公告)日:2004-09-01
  • US6972286B2
    申请人:——
    公开号:US6972286B2
    公开(公告)日:2005-12-06
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同类化合物

6-溴-3,4-二氢-2H-异硫代色烯-4-胺盐酸盐 6-溴-3,4-二氢-1H-S,S-二氧代异硫色烯-4-氨基盐酸盐 4-氨基异硫代苯并二氢吡喃2,2-二氧化物盐酸盐 3,4-二氢-1H-异硫苯并吡喃-4-胺盐酸盐 3,4-二氢-1H-S,S-二-氧代-异硫基苯并吡喃-4-胺盐酸盐 3,4-二氢-1H-2-苯并噻喃 2-异硫代苯并二氢吡喃-4-酮 1H-2-苯并噻喃-4-醇,3,4-二氢- (9ci)-3,4-二氢-1H-2-苯并硫代吡喃-1-羰酰氯 (4r)-(9ci)-6-乙基-3,4-二氢-1H-2-苯并硫代吡喃-4-胺,2,2-二氧化物 isothiochroman-1-yl-methyl-amine Isothiochroman-carbonsaeure-(1)-methylester 1-methyl-1H-2-benzothiopyran-1-carbonitrile 1-Methylenisothiochroman-2,2-dioxid 3,4-dihydro-1-vinyl-1H-2-benzothiopyran N-(2,4-Dinitro-phenyl)-N'-[(S)-1-methyl-isothiochroman-(4Z)-ylidene]-hydrazine 1,1'-Bis-(4,5-dihydro-1-oxy-2H-3-benzothiepin-3,3-dioxid)thiokohlensaeure-O,O-diester pyrrolidine-1-carboxylic acid isothiochroman-1-ylamide 1-(Chlormethyl)-isothiochroman-2,2-dioxid 4,5-Dihydro-2H-3-benzothiepin-1-on-2-thiocarbonsaeure-S-methylester isothiochroman-1-yl-carbamic acid ethyl ester piperidine-1-carbothioic acid isothiochroman-1-ylamide piperidine-1-carboxylic acid isothiochroman-1-ylamide 4,5-dihydro-benzo[d]thiepin-1-one semicarbazone 1-ethyl-3-isothiochroman-1-yl-thiourea 1-isothiochroman-1-yl-3-methyl-thiourea 2-(Methylen-dithiomethylen)-4,5-dihydro-2H-3-benzothiepin-1-on-3,3-dioxid 2-Benzyliden-4,5-dihydro-2H-3-benzothiepin-1-on methyl spiro[benzo[c]thiophene-1(3H),4'-piperidine]-1'-carboxylate 2,2-dioxide 1-hydroxy-3-isothiochroman-1-yl-urea 2-(N-p-Chlorphenyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on 1-isothiochroman-1-yl-3-methyl-urea di-isothiochroman-1-yl-amine 2-(N-Cyclohexyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on isothiochroman-1-yl-carbamic acid methyl ester 3-isothiochroman-1-yl-1,1-dimethyl-urea N-Isothiochroman-1-yl-N-methyl-formamide 2-(N-Phenyl-carbamoyl)-4,5-dihydro-2H-3-benzothiepin-1-on 4-isothiochroman-1-yl-semicarbazide 4,5-Dihydro-2H-3-benzothiepin-1-on-2-dithiocarbonsaeuremethylester 2-[2-Isothiochroman-(4Z)-ylidene-ethyl]-2-methyl-cyclopentane-1,3-dione 4-Hydroxy-4-vinylthiochroman 2-Methyl-2-{2-[6-methyl-isothiochroman-(4Z)-ylidene]-ethyl}-cyclopentane-1,3-dione 1-Methyl-1-carbamoyl-isothiochroman-2,2-dioxid 1-Deutero-1-cyano-isothiochroman morpholine-4-carbothioic acid isothiochroman-1-ylamide Dimethylaminomethyl-1-cyan-isothiochroman 1-Diethylaminomethyl-1-cyan-isothiochroman 2-Methyl-2-{2-[7-methyl-isothiochroman-(4Z)-ylidene]-ethyl}-cyclopentane-1,3-dione 55-((trimethylsilyl)ethynyl)-3,7-dithia-1(1,3),5(1,4)-dibenzenacyclooctaphane-12,15-dicarbonitrile