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-氨基-4,5-二氢-3-噻吩甲酰胺 | 133036-77-8

中文名称
2-氨基-4,5-二氢-3-噻吩甲酰胺
中文别名
——
英文名称
2-amino-4,5-dihydrothiophene-3-carboxamide
英文别名
2-amino-4,5-dihydro-3-thiophenecarboxamide;5-amino-2,3-dihydrothiophene-4-carboxamide
2-氨基-4,5-二氢-3-噻吩甲酰胺化学式
CAS
133036-77-8
化学式
C5H8N2OS
mdl
MFCD18819330
分子量
144.197
InChiKey
RYEIGLWKBYXZAT-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

物化性质

  • 熔点:
    138-139 °C(Solv: acetone (67-64-1))
  • 沸点:
    370.3±42.0 °C(Predicted)
  • 密度:
    1.393±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0
  • 重原子数:
    9
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    94.4
  • 氢给体数:
    2
  • 氢受体数:
    3

安全信息

  • 海关编码:
    2934999090

SDS

SDS:6764d450b45a8c87fccc59c77ada1284
查看

反应信息

  • 作为反应物:
    描述:
    2-氨基-4,5-二氢-3-噻吩甲酰胺吡啶硫酸氢铵四氯化锡 作用下, 以 1,4-二氧六环 为溶剂, 反应 22.0h, 生成 1H,3H-1-<(1,3-dihydroxy-2-propoxy)methyl>-5,6-dihydrothieno<2,3-d>pyrimidine-2,4-dione
    参考文献:
    名称:
    Synthesis and Antiviral Study of Dihydrothieno and Thianopyrimidine Diones Acyclic Nucleosides As Potential Anti-HIV Agents
    摘要:
    Acyclic nucleosides were prepared by alkylation of dihydrothieno and thianopyrimidines diones following Vorbruggen and Niedballa's method.((1))None of these HEPT analogues showed significant activity against Human Immunodeficiency Virus-1 (HIV-1).
    DOI:
    10.1080/15257779408011884
  • 作为产物:
    参考文献:
    名称:
    Maruoka, Hiroshi; Yamagata, Kenji; Yamazaki, Motoyoshi, Heterocycles, 1990, vol. 31, # 11, p. 2011 - 2023
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Synthesis and reactions of<i>n</i>-methyl-4-(methylthio)thieno[2,3-<i>d</i>]-pyrimidinium salts
    作者:Hiroshi Maruoka、Fumi Okabe、Kenji Yamagata
    DOI:10.1002/jhet.5570450543
    日期:2008.9
    the preparation of N-methyl-4-(methylthio)thieno[2,3-d]pyrimidinium salts 6a,b and 13a,b are described. Treatment of 6a,b and/or 13a,b with active methylene compounds such as malononitrile and ethyl cyanoacetate in the presence of sodium methoxide caused nucleophilic addition followed by elimination of methanethiol, giving the corresponding N-methyl-4-ylidenethieno[2,3-d]-pyrimidines 7a,b, 8a,b, 14a
    描述了两种制备N-甲基-4-(甲硫基)噻吩并[2,3- d ]嘧啶鎓盐6a,b和13a,b的方法。在甲醇钠存在下,用活性亚甲基化合物(如丙二腈和氰基乙酸乙酯)处理6a,b和/或13a,b引起亲核加成,然后消除甲硫醇,得到相应的N-甲基-4- yylenethieno [2,3 - d ] -pyrimidines 7A,7B,8A,8B,14A,b和15A,b 。
  • Synthesis of 2-amino-4,5-dihydro-3-methanesulfonylfurans (and -thiophenes)
    作者:Kenji Yamagata、Fumi Okabe、Hiroshi Maruoka、Yoshinobu Tagawa
    DOI:10.1002/jhet.5570420531
    日期:2005.7
    2-Amino-4,5-dihydro-3-methanesulfonylfurans 7 and 2-amino-4,5-dihydro-3-methanesulfonylthiophenes 8 were prepared by deamidation of tetrahydro-2-imino-3-methanesulfonyl-3-furancarboxamides 3 and of tetrahydro-2-imino-3-methanesulfonyl-3-thiophenecarboxamides 4 with bases. Compounds 3 and 4 were obtained by reaction of 2-amino-4,5-dihydro-3-furancarboxamides 1 and 2-amino-4,5-dihydro-3-thio-phenecarboxamides
    2-氨基-4,5-二氢-3- methanesulfonylfurans 7和2-氨基-4,5-二氢-3- methanesulfonylthiophenes 8是由四氢-2-亚氨基-3-甲磺酰基-3- furancarboxamides的脱酰胺化制备3的和具有碱的四氢-2-亚氨基-3-甲磺酰基-3-噻吩羧酰胺4。化合物3和4是在三乙胺存在下,使2-氨基-4,5-二氢-3-呋喃甲酰胺1和2-氨基-4,5-二氢-3-硫代苯甲酰胺2与甲磺酰氯反应制得的。
  • MARUOKA, HIROSHI;YAMAGATA, KENJI;YAMAZAKI, MOTOYOSHI, HETEROCYCLES, 31,(1990) N1, C. 2011-2023
    作者:MARUOKA, HIROSHI、YAMAGATA, KENJI、YAMAZAKI, MOTOYOSHI
    DOI:——
    日期:——
  • Maruoka, Hiroshi; Yamagata, Kenji; Yamazaki, Motoyoshi, Heterocycles, 1990, vol. 31, # 11, p. 2011 - 2023
    作者:Maruoka, Hiroshi、Yamagata, Kenji、Yamazaki, Motoyoshi
    DOI:——
    日期:——
  • Synthesis and Antiviral Study of Dihydrothieno and Thianopyrimidine Diones Acyclic Nucleosides As Potential Anti-HIV Agents
    作者:Jacques Renault、Daniel Laduree、Max Robba
    DOI:10.1080/15257779408011884
    日期:1994.6
    Acyclic nucleosides were prepared by alkylation of dihydrothieno and thianopyrimidines diones following Vorbruggen and Niedballa's method.((1))None of these HEPT analogues showed significant activity against Human Immunodeficiency Virus-1 (HIV-1).
查看更多

同类化合物

甲酰四硫富瓦烯 环己酮,2-[二(甲硫基)亚甲基]- 5-乙基-2-甲基-噻吩-3-酮 4-羟基-2,5-二甲基噻吩-3(2H)-酮 4-乙基硫烷基-丁-3-烯-2-酮 4,4-二甲基-1,1-双(甲基硫代)-1-戊烯-3-酮 3-[双(甲基磺酰基)亚甲基]-2,4-戊二酮 3,3-双(甲硫基)-2-氰基丙烯酸乙酯 2-氰基-3,3-双(甲基硫代)丙烯酰胺 2-氰-3,3-二(甲硫基)丙烯酸甲酯 2-氯-3-氧代-2,3-二氢-2-噻吩羧酸甲酯 2-氨基-4,5-二氢-3-噻吩甲酰胺 2-乙酰基-3-氨基-3-甲基硫代丙烯腈 2-丙烯酸,3-(十六烷基硫代)-,甲基酯,(Z)- 2-(环丙基羰基)-3,3-二(甲基硫代)丙烯腈 2-(1,3-二噻戊环-2-亚基)环戊酮 2-(1,3-二噻戊环-2-亚基)环己酮 2,2-二甲基噻吩-3-酮 1-己烯-3-酮,1,1-二(甲硫基)-2-硝基- 1,3-二硫杂环戊烯-4-羧酸 (3Z)-1,1,1-三氟-4-(甲硫基)-3-丁烯-2-酮 (3E)-4-(甲硫基)-3-戊烯-2-酮 (2Z)-[3-(2-溴乙基)-4-氧代-1,3-噻唑烷-2-亚基]乙酸乙酯 (2Z)-2-(3-乙基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2Z)-(3-甲基-4-氧代-1,3-噻唑烷-2-亚基)乙酸乙酯 (2E)-2-(4-氧代噻唑烷-2-亚基)乙酸丁酯 2-[bis(methylthio)methylene]-5-([13C]-methyl)cyclohexanone 2-Cyan-2-(2,3,4,5,6,7-hexahydrobenzothiazol-2-yliden)essigsaeuremethylester 2-(chlorodifluoromethylcarbonylmethylene)-1,3-thiazolidine 2,3-bis((S)-2-dodecyloxy-propanylthio)-6-(carboxy)tetrathiafulvalene 3-Amino-2-cyan-3-(ethylthio)acrylsaeuremethylester 5-dimethylaminomethylene-3-ethoxycarbonyl-2-methyl-4-oxo-4,5-dihydrothiophene 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-dithiolane 2-(1-methoxycarbonyl)trifluoroethylidene-1,3-oxathiolane (Z)-4-(1-Butylthio)-but-3-en-2-one methyl 3-(butylthio)acrylate 3-Methylamino-3-methylmercapto-2-cyan-acrylsaeure-methylester 2-sec-butoxy-3,5-dimethylthiotetronic acid ethyl 2-amino-4-hydroxy-5-methyl-4-(trifluoromethyl)-4,5-dihydrothiophene-3-carboxylate cyano-(3-ethyl-4-oxo-thiazolidin-2-yliden)-acetic acid allyl ester 2‑(3,3‑dimethyl‑2‑oxobutylidene)‑1,3‑thiazolidin‑4‑one isopropyl 1,3-dithiol-2-ylidenemethylsulfonylacetate (E)-5-(furan-2-yl)-1,1-bis(methylthio)penta-1,4-dien-3-one ethyl 3-cyclohexylamino-3-methylthio-2-cyanoacrylate ethyl 2-ethoxy-4,5-dihydrothiophene-3-carboxylate 2,4-dimethyl-2,3-dihydro-thiophen-3-one isopropyl 2-(1,3-dithiol-2-ylidene)-2-(N-cyclohexylcarbamoyl)acetate 4,4-bis(methylthio)but-3-en-2-one-1,1,1,3-d4 N-(2-aminoethyl)-benzo[b]thieno[2,3-c]pyridine-3-carboamide.hydrochloride 3-(1,3-dithiolan-2-ylidene)butan-2-one