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3-amino-7-methyl-1-thioxo-5,6,7,8-tetrahydro-1H-isothiochromene-4-carbonitrile

中文名称
——
中文别名
——
英文名称
3-amino-7-methyl-1-thioxo-5,6,7,8-tetrahydro-1H-isothiochromene-4-carbonitrile
英文别名
3-Amino-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromene-4-carbonitrile
3-amino-7-methyl-1-thioxo-5,6,7,8-tetrahydro-1H-isothiochromene-4-carbonitrile化学式
CAS
——
化学式
C11H12N2S2
mdl
——
分子量
236.362
InChiKey
BSYKZSVNDPVEGB-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):
    2.6
  • 重原子数:
    15
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    107
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    3-amino-7-methyl-1-thioxo-5,6,7,8-tetrahydro-1H-isothiochromene-4-carbonitrilesodium acetate一水合肼 作用下, 以 乙醇 为溶剂, 反应 17.5h, 生成 ethyl 7-amino-10-methyl-8,9,10,11-tetrahydrothieno[2,3-c][1,2,4]triazolo[3,4-a]isoquinoline-6-carboxylate
    参考文献:
    名称:
    基于稠合吡啶硫酮的肼衍生物合成四环噻吩并三唑并吡啶
    摘要:
    开发了一种基于脂环酮和杂环酮的稠合吡啶硫酮肼衍生物的合成方法。对这些肼衍生物进行连续杂环化以获得三环三唑并[4,3- a ]吡啶、四环噻吩并[3,2 -e ][1,2,4]三唑并[ 4,3- a ]的新衍生物]吡啶,以及噻吩并[2,3 - c ][1,2,4]三唑并[3,4- a ]-2,7-萘啶的新杂环体系。
    DOI:
    10.1007/s11172-022-3503-5
  • 作为产物:
    描述:
    二硫化碳4-甲基环己酮丙二腈三乙胺 作用下, 以 乙醇 为溶剂, 反应 48.0h, 以73.4%的产率得到3-amino-7-methyl-1-thioxo-5,6,7,8-tetrahydro-1H-isothiochromene-4-carbonitrile
    参考文献:
    名称:
    基于稠合吡啶硫酮的肼衍生物合成四环噻吩并三唑并吡啶
    摘要:
    开发了一种基于脂环酮和杂环酮的稠合吡啶硫酮肼衍生物的合成方法。对这些肼衍生物进行连续杂环化以获得三环三唑并[4,3- a ]吡啶、四环噻吩并[3,2 -e ][1,2,4]三唑并[ 4,3- a ]的新衍生物]吡啶,以及噻吩并[2,3 - c ][1,2,4]三唑并[3,4- a ]-2,7-萘啶的新杂环体系。
    DOI:
    10.1007/s11172-022-3503-5
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文献信息

  • Synthesis of tetracyclic thienotriazolopyridines based on hydrazine derivatives of fused pyridinethiones
    作者:E. G. Paronikyan、Sh. Sh. Dashyan、A. S. Harutyunyan、S. S. Mamyan、E. S. Safaryan
    DOI:10.1007/s11172-022-3503-5
    日期:2022.5
    method for the synthesis of hydrazine derivatives of fused pyridinethiones based on alicyclic and heterocyclic ketones has been developed. Successive heterocyclization of these hydrazine derivatives was carried out in order to obtain new derivatives of tricyclic triazolo[4,3-a]pyridines, tetracyclic thieno[3,2-e][1,2,4]triazolo[4,3-a]pyridines, as well as a new heterocyclic system of thieno[2,3-c][1,2
    开发了一种基于脂环酮和杂环酮的稠合吡啶硫酮肼衍生物的合成方法。对这些肼衍生物进行连续杂环化以获得三环三唑并[4,3- a ]吡啶、四环噻吩并[3,2 -e ][1,2,4]三唑并[ 4,3- a ]的新衍生物]吡啶,以及噻吩并[2,3 - c ][1,2,4]三唑并[3,4- a ]-2,7-萘啶的新杂环体系。
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同类化合物

4-甲基-6-硫氧代-3,6-二氢-2H-1,3-噻嗪-2-酮 2H-噻喃-2-硫酮,3,5-二甲基- 2-噻丁环硫酮,3,3-二甲基-4-(1-甲基亚乙基)- 1H-2-苯并硫代吡喃-4-甲腈,5,6,7,8-四氢-3-氨基-1-硫代- 2-Amino-4-(2-furyl)-6H-1,3-thiazinthion-(6) 2-amino-4-propyl-[1,3]thiazine-6-thione bis(ethylenedithio)tetrathiafulvalenothioquinone-1,3-dithiolemethide 1,5,6,7-tetrahydrocyclopenta<1,3>thiazine-2,4-dithione 3-Amino-6,6-dimethyl-1-thioxo-5,8-dihydro-1H,6H-thiopyrano[3,4-c]thiopyran-4-carbonitrile 2-Amino-4-methyl-6H-1,3-thiazinthion-(6) 2-amino-4-(2-(thienyl)-1,3-thiazine-6-thione ethylenedithio-tetrathiafulvalenothioquinone-1,3-diselenolemethide 4-Methylidenethietane-2-thione 3,4-trimethylene-6-amino-5-ethoxycarbonyl-2(1H)thiopyranethione Dithiolactone 2 methyl 2-thioxo-2H-thiopyran-5-carboxylate 3-Ethyl-3-methyl-3H-thiophene-2-thione Thiopyran-2-thion 1H,8H-pyrido[4,3-d][1,3]thiazine-2,4,5,7-tetrathione 6-amino-3,3-dimethyl-8-sulfanylidene-1H,3H,4H,8H-thiopyrano[3,4-c]pyran-5-carbonitrile 3-amino-1-thioxo-1,5,6,7-tetrahydrocyclopenta[c]thiopyran-4-carbonitrile methyl 3-methyl-5-(perfluoropentyl)-2-thioxo-2,3-dihydrothiophene-3-carboxylate 3H-thiophene-2-thione 3-amino-6,6-dimethyl-1-thioxo-1,5,6,7-tetrahydrocyclopenta[c]thiopyran-4-carbonitrile 3-(aminomethylidene)-5-ethylthiophene-2-thione 5-ethyl-3-[[2-[(5-ethyl-2-sulfanylidenethiophen-3-ylidene)methylamino]ethylamino]methylidene]thiophene-2-thione (3E)-5-ethyl-3-[[2-[[(E)-(5-ethyl-2-sulfanylidenethiophen-3-ylidene)methyl]amino]ethylamino]methylidene]thiophene-2-thione ethyl N-[(7S)-4-cyano-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromen-3-yl]carbamate 2-(4,5-Diethyl-1,3-dithiol-2-ylidene)-5-sulfanyl-1,3-dithiolane-4-thione (3E)-3-(aminomethylidene)-5-ethylthiophene-2-thione (3Z)-3-(aminomethylidene)-5-ethylthiophene-2-thione (3Z)-5-ethyl-3-[[2-[[(Z)-(5-ethyl-2-sulfanylidenethiophen-3-ylidene)methyl]amino]ethylamino]methylidene]thiophene-2-thione 12-[4-(12-Sulfanylidene-1,4,7-trioxa-10,13-dithiacyclopentadec-11-ylidene)-1,3-dithietan-2-ylidene]-1,4,7-trioxa-10,13-dithiacyclopentadecane-11-thione ethyl N-[(7R)-4-cyano-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromen-3-yl]carbamate butyl N-[(7S)-4-cyano-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromen-3-yl]carbamate butyl N-[(7R)-4-cyano-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromen-3-yl]carbamate propyl N-[(7S)-4-cyano-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromen-3-yl]carbamate 3-amino-7-methyl-1-thioxo-5,6,7,8-tetrahydro-1H-isothiochromene-4-carbonitrile 4,6-diamino-2-thioxo-2H-thiopyran-3,5-dicarbonitrile 1-(2-sulfanylidene-3H-thiophen-5-yl)ethanone 7-methyl-4,5-dihydro-3H-thiepine-2-thione 1H-pyrazolo[3,4-d][1,3]thiazine-4-thione 1-(2-sulfanylidene-3H-thiophen-4-yl)propan-2-one 1,4-Dithiine-2-thione 5-Sulfanyl-1,3-dithiolane-4-thione 2,2-dimethyl-1-(2-sulfanylidene-3H-thiophen-5-yl)propan-1-one (3R)-6-amino-3-ethyl-3-methyl-8-sulfanylidene-1,4-dihydrothiopyrano[3,4-c]pyran-5-carbonitrile (3S)-6-amino-3-ethyl-3-methyl-8-sulfanylidene-1,4-dihydrothiopyrano[3,4-c]pyran-5-carbonitrile (7S)-3-amino-7-methyl-1-sulfanylidene-5,6,7,8-tetrahydroisothiochromene-4-carbonitrile 3-amino-1-sulfanylidene-6,7,8,9-tetrahydro-5H-cyclohepta[c]thiopyran-4-carbonitrile