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N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]-thio]ethyl]thieno[3,4-d]isothiazol-3-amine 1,1-dioxide | 94662-50-7

中文名称
——
中文别名
——
英文名称
N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]-thio]ethyl]thieno[3,4-d]isothiazol-3-amine 1,1-dioxide
英文别名
N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]thio]ethyl]thieno[3,4-d]isothiazole-3-amine 1,1-dioxide;Thieno(3,4-D)isothiazol-3-amine, N-(2-(((5-((dimethylamino)methyl)-2-furanyl)methyl)thio)ethyl)-, 1,1-dioxide;1-[5-[2-[(1,1-dioxothieno[3,4-d][1,2]thiazol-3-ylidene)amino]ethylsulfanylmethyl]furan-2-yl]-N,N-dimethylmethanamine
N-[2-[[[5-[(Dimethylamino)methyl]-2-furanyl]methyl]-thio]ethyl]thieno[3,4-d]isothiazol-3-amine 1,1-dioxide化学式
CAS
94662-50-7
化学式
C15H19N3O3S3
mdl
——
分子量
385.532
InChiKey
CPQCBGMVDITBNW-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:
    106-109 °C
  • 沸点:
    536.5±60.0 °C(Predicted)
  • 密度:
    1.46±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    24
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    137
  • 氢给体数:
    1
  • 氢受体数:
    7

SDS

SDS:422d3f6d344e4d9a4f62253f4461140f
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反应信息

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文献信息

  • Process for preparing thieno-fused heterocyclic anti-ulcer agents and
    申请人:American Home Products Corporation
    公开号:US04622402A1
    公开(公告)日:1986-11-11
    A process for preparing certain thieno-fused heterocyclic compounds having H.sub.2 -receptor antagonist and antisecretory activity, which involves the reaction of a mercaptan, obtained by reduction of a thienoisothiazole amino alkyl disulfide, with a 5-substituted-2-furanylmethanol; and said thienoisothiazole amino alkyl disulfide intermediates.
    一种制备具有H.sub.2-受体拮抗剂和抗分泌活性的某些噻吩-融合杂环化合物的过程,涉及将由还原噻吩异硫氰酸酯氨基烷基二硫化物得到的巯基化合物与5-取代-2-呋喃甲醇反应;以及所述的噻吩异硫氰酸酯氨基烷基二硫化物中间体。
  • Benzo-fused heterocyclic anti-ulcer agents
    申请人:American Home Products Corporation
    公开号:US04490527A1
    公开(公告)日:1984-12-25
    Compounds of the formula: ##STR1## wherein B is a moiety having the formula: ##STR2## R is mono- or dihalo, amino, nitro, cyano, hydroxy, trifluoromethyl, mercapto, lower alkyl, lower alkoxy, alkanoyl, cycloalkyl of 4-7 carbon atoms, carboxy, alkoxycarbonyl, mono- or di-lower alkyl substituted amino, alkanoylamino, lower alkyl thio, lower alkylsulfonyl, sulfamoyl, lower alkyl substituted sulfamoyl, phenyl or phenyl substituted with halo, lower alkyl, lower alkoxy, trifluoromethyl, hydroxy, amino, cyano or nitro. X is SO.sub.2, SO, S or C.dbd.O; and A is amine selected from the group ##STR3## , wherein R.sup.1 is hydrogen or R.sup.2 CH.sub.2 wherein R.sup.2 is mono- or diloweralkylamino, mono- or di-N-lower alkylaminoloweralkyl, (2-furyl)methylamino, benzylamino, lowercycloalkylamino, 1-pyrrolidinyl, 1-piperidinyl, 1-hexahydroazepinyl, 1-octahydroazocinyl, 3-thiazolidinyl, 4-morpholinyl or 4-thiomorpholinyl; R.sup.3 is hydrogen or (1-piperidinyl)methyl with the proviso that when R.sup.3 is (1-piperidinyl)methyl, R.sup.1 is hydrogen; n is 1 to 4, and the pharmacologically acceptable salts thereof.
    该化合物的公式为:##STR1## 其中B是具有以下式子的基团:##STR2## R是单卤素或双卤素,氨基,硝基,氰基,羟基,三氟甲基,巯基,较低烷基,较低烷氧基,烷酰基,碳数为4-7的环烷基,羧基,烷氧羰基,单或双较低烷基取代的氨基,烷酰氨基,较低烷基硫基,较低烷基磺酰基,磺酰胺基,较低烷基取代的磺酰胺基,苯基或取代有卤素,较低烷基,较低烷氧基,三氟甲基,羟基,氨基,氰基或硝基的苯基。X为SO.sub.2,SO,S或C.dbd.O;A是从以下组中选择的胺基:##STR3## 其中R.sup.1是氢或R.sup.2 CH.sub.2,其中R.sup.2是较低烷基氨基,单或双N-较低烷基氨基较低烷基,(2-呋喃基)甲基氨基,苄基氨基,较低环烷基氨基,1-吡咯基,1-哌啶基,1-六氢-杂环庚基,1-八氢-杂环十二烷基,3-噻唑烷基,4-吗啉基或4-硫代吗啉基;R.sup.3是氢或(1-哌啶基)甲基,但当R.sup.3是(1-哌啶基)甲基时,R.sup.1为氢;n为1-4,以及其药学上可接受的盐。
  • Fused heterocyclic compounds
    申请人:AMERICAN HOME PRODUCTS CORPORATION
    公开号:EP0120585B1
    公开(公告)日:1987-12-16
  • SANTILLI, ARTHUR A.;SCOTESE, ANTHONY C.;MORRIS, ROBERT L.;NIELSEN, SUSAN +, EUR. J. MED. CHEM., 24,(1989) N, C. 87-90
    作者:SANTILLI, ARTHUR A.、SCOTESE, ANTHONY C.、MORRIS, ROBERT L.、NIELSEN, SUSAN +
    DOI:——
    日期:——
  • ——
    作者:SCHIEHSER G. A.、 STRIKE D. P.
    DOI:——
    日期:——
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同类化合物

噻吩并[3,2-d]异噻唑-5-羧酸乙酯 5-苯基-3-(1H-吡唑-1-基)噻吩并[2,3-d]异噻唑1,1-二氧化 4-氯-8-(甲基硫烷基)异噻唑并[4',5':4,5]噻吩并[3,2-d][1,2,3]三嗪 4-氨基-3-甲硫基噻吩并[4,5-d][1,2]噻唑-5-甲酰胺 4-氨基-3-甲基噻吩并[2,3-c]异噻唑-5-羧酸乙酯 4-氨基-3-[(4-氟苯甲基)硫烷基]噻吩并[2,3-c]异噻唑-5-甲酰胺 4-[2-(6-甲氧基萘-2-基)丙基]-N-甲基哌嗪-1-甲酰胺 4,6-二氢噻吩并[3,4-d][1,3]噻唑5,5-二氧化物 3-甲基噻吩并[2,3-c]异噻唑-5-羧酸乙酯 3-(4-氯-3,5-二甲基-1H-吡唑-1-基)噻吩并[3,4-d]异噻唑1,1-二氧化 3-(4-氯-1H-吡唑-1-基)噻吩并[3,4-d]异噻唑1,1-二氧化 3-(3,5-二甲基吡唑-1-基)噻吩并[3,4-d][1,2]噻唑1,1-二氧化物 2-甲基噻吩并噻唑 2-甲基噻吩并[2,3-d]异噻唑-3(2H)-酮 1,1-二氧化物 2-氨基噻吩并[2,3-d]噻唑-6-羧酸 甲酯 2-氨基噻吩并[2,3-D]噻唑 1,1-二氧代噻吩并[2,3-D]异噻唑-3-酮 (9CI)-2-氨基-噻吩并[2,3-d]噻唑-5-羧酸 5-acetyl-3-phenylthieno<3,2-d>isothiazole 3-phenylthienol<3,2-d>isothiazol-4(5H)-one 5-bromo-3-phenylthieno<3,2-d>isothiazole 5-methyl-2-(2-(pyridin-2-yl)propan-2-yl)thieno[2,3-d]isothiazol-3(2H)-one cis-2-α-methylbenzylidenehydrazonoperhydrothieno<3,4-d>thiazole-5,5-dioxide 3-(4-Chlorophenyl)-5-(4-methylphenyl)-2,3-dihydro-2-thioxothieno[2,3-d]thiazole 3-Phenyl-5-(4-methylphenyl)-2,3-dihydro-2-thioxothieno[2,3-d]thiazole 3,5-Di(4-methylphenyl)-2,3-dihydro-2-thioxothieno[2,3-d]thiazole 3-(4-Methylphenyl)-5-(4-bromophenyl)-2,3-dihydro-2-thioxothieno[2,3-d]thiazole (E)-2,3-Dihydro-2-methyl-3-ethyliden-thieno<3,2-d>isothiazol-1,1-dioxid (Z)-2,3-Dihydro-2-methyl-3-ethyliden-thieno<3,2-d>isothiazol-1,1-dioxid (E)-2,3-Dihydro-2-methyl-3-ethyliden-thieno<2,3-d>isothiazol-1,1-dioxid (Z)-2,3-Dihydro-2-methyl-3-ethyliden-thieno<2,3-d>isothiazol-1,1-dioxid 3-Ethylthio-thieno<3,2-d>isothiazol-1,1-dioxid 6-chloro-2-methylthieno[3,2-d]thiazole 3-Ethylthio-thieno<2,3-d>isothiazol-1,1-dioxid 5-(4-bromophenyl)-2,3-dihydro-2-phenyliminothieno[2,3-d]thiazole 7-Ethyl-2-amino-6,7,8,9-tetrahydro-5H-thiazolo(4',5':5,4)thieno(2,3-d)azepine dihydrochloride 2,4-Dimethyl-thieno[3,4-d]thiazole 4-Methyl-2-phenylthieno[3,4-d][1,3]thiazole 5-(4-chlorophenyl)-2,3-dihydro-2-phenyliminothieno[2,3-d]thiazole 6-(4-methoxy-phenyl)-thieno[3,4-d]thiazole 5-phenyl-2,3-dihydro-2-phenyliminothieno[2,3-d]thiazole 2,3-Dihydro-2,5-dimethyl-3-oxo-thieno<3,2-d>isothiazol-1,1-dioxid 2,3-Dihydro-5-methyl-3-oxothieno<3,2-d>isothiazole 1,1-dioxide 5-Ethoxycarbonyl-6-hydroxy-2-oxo-3-phenyl-2,3-dihydrothieno<2.3-d>-1,3-thiazol 2-(2-ethylhexyl)thieno[3,4-d]thiazole 4,6-dibromo-2-(2-ethylhexyl)thieno[3,4-d]thiazole ethyl 6-amino-2-chlorothieno<2,3-d>thiazole-5-carboxylate methyl 6-methyl-2-(methylsulfanyl)thieno[2,3-d]thiazole-5-carboxylate methyl 6-methyl-2-(pyrrolidin-1-yl)thieno[2,3-d]thiazole-5-carboxylate methyl 6-methyl-2-morpholinothieno[2,3-d]thiazole-5-carboxylate