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2-(thiophen-3-yl)-4,5-dihydro-1,3-thiazole | 1318795-40-2

中文名称
——
中文别名
——
英文名称
2-(thiophen-3-yl)-4,5-dihydro-1,3-thiazole
英文别名
2-Thiophen-3-yl-4,5-dihydro-1,3-thiazole
2-(thiophen-3-yl)-4,5-dihydro-1,3-thiazole化学式
CAS
1318795-40-2
化学式
C7H7NS2
mdl
——
分子量
169.271
InChiKey
WIGNXBSYICAEJH-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):
    1.7
  • 重原子数:
    10
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.29
  • 拓扑面积:
    65.9
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    2-溴乙胺氢溴酸盐噻吩-3-硫代酰胺sodium carbonate 作用下, 以 为溶剂, 反应 2.0h, 以81%的产率得到2-(thiophen-3-yl)-4,5-dihydro-1,3-thiazole
    参考文献:
    名称:
    Easy access to thiazolines and thiazines via tandem S-alkylation-cyclodeamination of thioamides/haloamines
    摘要:
    这是首次报道通过硫代酰胺/卤胺的自催化、水辅助串联 S-烷基化-环脱氨基反应简便合成噻唑啉类和噻嗪类化合物。该反应清洁高效,产物处理简单,适用于多种底物。
    DOI:
    10.1039/c1gc15285h
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文献信息

  • Peptide compound and method for producing same, composition for screening use, and method for selecting peptide compound
    申请人:FUJIFILM Corporation
    公开号:US11319347B2
    公开(公告)日:2022-05-03
    An object of the present invention is to provide a novel cyclic peptide compound excellent in cell membrane permeability, a method for producing the same, a composition for screening use, and a method for selecting a cyclic peptide compound that binds to a target substance. According to the present invention, a peptide compound represented by Formula (1) or a salt thereof is provided. In the formula, the symbols have the meanings as defined in the specification of the present application.
    本发明的目的是提供一种细胞膜渗透性极佳的新型环肽化合物、一种生产该化合物的方法、一种用于筛选的组合物以及一种选择与目标物质结合的环肽化合物的方法。根据本发明,提供了一种由式(1)表示的多肽化合物或其盐。式中的符号具有本申请说明书中定义的含义。
  • PEPTIDE COMPOUND AND METHOD FOR PRODUCING SAME, COMPOSITION FOR SCREENING USE, AND METHOD FOR SELECTING PEPTIDE COMPOUND
    申请人:FUJIFILM Corporation
    公开号:US20200040039A1
    公开(公告)日:2020-02-06
    An object of the present invention is to provide a novel cyclic peptide compound excellent in cell membrane permeability, a method for producing the same, a composition for screening use, and a method for selecting a cyclic peptide compound that binds to a target substance. According to the present invention, a peptide compound represented by Formula (1) or a salt thereof is provided. In the formula, the symbols have the meanings as defined in the specification of the present application.
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同类化合物

替莫美他汀 乙酰亚胺基硫酸,甲基酯 S-甲基-N,N-二甲基硫代乙酰胺碘化物 5-甲基四氢噻吩-2-亚胺盐酸盐 4-[(1E,5E,7E,11R)-11-甲氧基十四碳-1,5,7,13-四烯基]-2-(2-甲基环丙基)-4,5-二氢-1,3-噻唑 2-环戊基-4,5-二氢-1,3-噻唑 2-氧代丙基乙烷硫代亚氨酸酯 2-亚氨基硫烷盐酸盐 2-亚氨基硫杂环戊烷 2-亚氨基-5-甲基-3-(3-氧代丁基)四氢-3-噻吩甲腈 2-亚氨基-4-氧代四氢-3-噻吩羧酸 2-亚氨基-2-(甲基硫代)乙酸乙酯 2-亚氨基-2,3-二氢-噻吩 1-[5-(甲硫基)-3,4-二氢-2H-吡咯-3-基]乙酮 (S)-5-乙基-2-硫代甲基-1-吡咯啉 (4R)-4-[(1Z,5E,7E,11R)-11-甲氧基-8-甲基十四碳-1,5,7,13-四烯基]-2-[(1R,2S)-2-甲基环丙基]-4,5-二氢-1,3-噻唑 (3,6-二碘噻吩并[3,2-b]噻吩e-2,5-二亚基)二氰胺 N-Ethyl-thiopropionimidic acid methyl ester 3-Methylene-6-[1-methylsulfanyl-meth-(E)-ylidene]-oxepane (Z)-2-Methylsulfanyl-azacyclotridec-1-ene (E)-12-Methylsulfanyl-azacyclododec-12-ene 1-<5-Aethyl-3-butylmercapto-<1,2,4>triazol-4-yl>-2-mercapto-4,4,6-trimethyl-1,4-dihydropyrimidin N-Ethyl-thioacetimidic acid methyl ester (E)-10-Methylsulfanyl-2,3,4,5,6,7,8,9-octahydro-azecine N-Ethyl-thiopropionimidic acid methyl ester 1-Pyrrolin-2-ylmercapto>-essigsaeure-tert.-butylester 2,2,2-Trichloro-thioacetimidic acid butyl ester 2-Ethyl-2,3,4,7-tetramethyl-8-acetyl-2H,6H-pyrimido<2,1-b>-1,3-thiazin 8-Ethylsulfanyl-6-methyl-7-aza-bicyclo[4.2.0]octa-3,7-diene Thioisobutyrimidic acid methyl ester; hydriodide N-Ethyl-2-methyl-buta-2,3-dienimidothioic acid methyl ester 1-(3-(bis(dimethylamino)methyl)-2-(ethylimino)-2,3-dihydro-4-methylthiazol-5-yl)ethanone chloride 1,3,5-tris[2-(4S)-4-i-propyl-1,3-thiazolin-2-yl]benzene 4-(1'-hydroxyiminoethyl)-4-methyl-1,3-dithiolan-2-ylidenemalononitrile chloro-[(E)-3-methoxy-1-thiocyanatoprop-1-en-2-yl]mercury 3-{5-[3-Methyl-5-methylsulfanyl-3H-[1,3,4]thiadiazol-(2Z)-ylidene]-4-oxo-2-thioxo-thiazolidin-3-yl}-propionic acid 4-(dimethylamino)-2-methylsulfanyl-1,4-diazabuta-1,3-dienium iodide 2-methylsulfanyl-azacyclotridec-1-ene 2-Cyano-3-trimethylsilanylmethylsulfanyl-thiopropionimidic acid trimethylsilanylmethyl ester; hydrochloride isopropyl methyl cyanocarbonimidodithioate 2,4-bis-methylsulfanyl-1,3-diaza-spiro[4.5]deca-1,3-diene 9-methylsulfanyl-3,4,5,6,7,8-hexahydro-2H-azonine 1,1,2-Trimethyl-4-n-butyl-S-methyl-isothiosemicarbazid 2-chloroallyl methyl cyanocarbonimidodithioate S-(3-azido-2,2-dimethylpropyl) ethanethioate [Methylsulfanyl(prop-2-enylsulfanyl)methylidene]cyanamide 2,3-bis(4-fluorobutylthio)maleonitrile 7-(methylsulfanyl)-8-methoxy-6-azaspiro-[4.5]deca-6,8-diene