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7-tert-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene

中文名称
——
中文别名
——
英文名称
7-tert-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene
英文别名
7-tert.-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene;7-t-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene;3-methyl-7-[(2-methylpropan-2-yl)oxycarbonylamino]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid
7-tert-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene化学式
CAS
——
化学式
C13H18N2O5S
mdl
——
分子量
314.362
InChiKey
MIQOWEPEDFRWDS-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):
    1.15
  • 重原子数:
    21.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    95.94
  • 氢给体数:
    2.0
  • 氢受体数:
    5.0

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    7-tert-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene二苯基重氮甲烷乙酸乙酯盐酸Sodium sulfate-III甲烷环己烷乙醚 、 crystals 作用下, 以 乙腈 为溶剂, 22.0~40.0 ℃ 、355.5 kPa 条件下, 反应 16.75h, 以2-Benzhydryloxycarbonyl-7-tert.butoxycarbonylamino-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (191 g) is obtained in the form of white crystals (m.p.=179° C.)的产率得到2-Benzhydryloxycarbonyl-7-tert-butoxycarbonylamino-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene
    参考文献:
    名称:
    3-Vinyl-cephalosporins
    摘要:
    式为##STR1##的新型3-乙烯基头孢菌素,其中n为0或1,R.sub.1为氢,式为##STR2##的基团[其中R.sub.4为氢或保护基团,R.sub.5为氢、烷基、乙烯基或氰甲基或为保护基团],或保护基团,R.sub.2为氢、保护基团或酶可去除的基团,或R.sub.1为氢或可携带各种取代基的酰基基团,R.sub.2为氢或保护基团,R.sub.3为一般式R'.sub.3--SO.sub.2--O--或R".sub.3--CO--O--的基团,其中R'.sub.3为烷基、三氟甲基、三氯甲基或被卤素原子、烷基或硝基基团取代的苯基,R".sub.3的定义与R'.sub.3相同或代表被酰基或烷氧羰基取代的甲基,或代表2-位被酰基或烷氧羰基取代的乙基或丙基。这些化合物可用作制备抗生素3-硫代乙烯基头孢菌素的中间体。
    公开号:
    US04307230A1
  • 作为产物:
    描述:
    二碳酸二叔丁酯7-氨基去乙酰氧基头孢烷酸乙酸乙酯氯化钠Sodium sulfate-III 作用下, 以 碳酸氢钠1,4-二氧六环 为溶剂, 25.0~50.0 ℃ 、355.5 kPa 条件下, 反应 48.17h, 以7-tert.-Butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene (486 g) is obtained in the form of yellow crystals (m.p.=190° C., with decomposition)的产率得到7-tert-butoxycarbonylamino-2-carboxy-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene
    参考文献:
    名称:
    3-Thiovinyl-cephalosporins
    摘要:
    通式(I)的新型头孢菌素;其中R为烷基,L-2-氨基-2-羧基乙基,苯基,吡啶基,吡啶-N-氧化物,嘧啶-2-基,取代的吡啶-3-基,4-位取代的5,6-二氧化-1,4,5,6-四氢-1,2,4-三嗪-3-基,1,3,4-三唑-5-基或1-位取代的2-烷氧羰基-1,3,4-三唑-5-基,1,4-二烷基-5,6-二氧化-1,4,5,6-四氢-1,2,4-三嗪-3-基,1-烷基-5,6-二氧化-1,4,5,6-四氢-1,2,4-三嗪-3-基,2-烷基-5,6-二氧化-1,2,5,6-四氢-1,2,4-三嗪-3-基,三唑-5-基,1,3,4-噻二唑-5-基,取代或未取代的1,2,4-噻二唑-5-基,取代或未取代的1,3,4-噁二唑-5-基,取代或未取代的噁唑-2-基或取代或未取代的1-位四唑-5-基,R'为氢原子或通式(II)的基团;其中R.sup.o为氢,烷基,乙烯基或氰甲基,以及它们的盐,可用作抗菌剂。
    公开号:
    US04307116A1
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文献信息

  • 3-Vinyl-cephalosporin derivatives
    申请人:Rhone-Poulenc Industries
    公开号:US04307233A1
    公开(公告)日:1981-12-22
    Novel 3-vinyl-cephalosporin derivates of the general formula ##STR1## in the bicyclooct-2-ene or bicyclooct-3-ene form, in which R.sub.1 is a protective radical or is a radical of the general formula ##STR2## in which R.sub.5 is hydrogen, alkyl, vinyl or cyanomethyl, or a protective radical, and R.sub.6 is hydrogen or a protective radical, and R.sub.2 is a protective radical or an enzymatically removable radical, or R.sub.1 is an acyl radical, which may carry various substituents, and R.sub.2 represents a protective radical, and R.sub.3 and R.sub.4, which are identical or different, represent alkyl (optionally substituted by hydroxyl, alkoxy, amino, alkylamino or dialkylamino) or phenyl, or form, together with the nitrogen atom, a saturated 5-membered or 6-membered heterocyclic ring optionally containing another hetero-atom, their E- and Z-forms and their mixtures, are useful as intermediates for the preparation of 3-thiovinyl cephalosporins useful as antibacterial agents.
    具有通式##STR1##的新型3-乙烯基头孢菌素衍生物,以双环辛-2-烯或双环辛-3-烯形式存在,其中R1为保护基团或具有通式##STR2##的基团,其中R5为氢、烷基、乙烯基或氰甲基,或为保护基团,R6为氢或保护基团,R2为保护基团或酶可去除的基团,或R1为可带有各种取代基的酰基基团,R2表示保护基团,R3和R4相同或不同,表示烷基(可被羟基、烷氧基、氨基、烷基氨基或二烷基氨基取代)或苯基,或与氮原子一起形成含有另一个杂原子的饱和5元或6元杂环环,它们的E型和Z型及其混合物,可作为制备作为抗菌剂有用的3-硫代乙烯基头孢菌素的中介体。
  • 3-Vinyl-cephalosporins
    申请人:Rhone-Poulenc Industries
    公开号:US04307230A1
    公开(公告)日:1981-12-22
    Novel 3-vinyl-cephalosporins of the formula ##STR1## in which n is 0 or 1, R.sub.1 is hydrogen, a radical of the formula ##STR2## [in which R.sub.4 is hydrogen or a protective radical and R.sub.5 is hydrogen, alkyl, vinyl or cyanomethyl or is a protective radical], or a protective radical, and R.sub.2 is hydrogen, a protective radical or an enzymatically removable radical, or R.sub.1 is hydrogen or an acyl radical which may carry various substituents and R.sub.2 is hydrogen or a protective radical, and R.sub.3 is a radical of the general formula R'.sub.3 --SO.sub.2 --O-- or R".sub.3 --CO--O--, in which R'.sub.3 is alkyl, trifluoromethyl, trichloromethyl or phenyl which is substituted by a halogen atom or by an alkyl or nitro radical, and R".sub.3 is defined like R'.sub.3 or represents methyl which is substituted by acyl or alkoxycarbonyl, or represents ethyl or propyl substituted in the 2-position by acyl or alkoxycarbonyl. These compounds are useful as intermediates for the preparation of antibiotic 3-thiovinyl-cephalosporins.
    新型3-乙烯基头孢菌素化合物,其通式为##STR1##,其中n为0或1,R1为氢、通式##STR2##的基团[其中R4为氢或保护基团,R5为氢、烷基、乙烯基或氰甲基或为保护基团],或为保护基团,R2为氢、保护基团或酶可去除的基团,或者R1为氢或可能带有各种取代基的酰基基团,R2为氢或保护基团,R3为一般通式R'3--SO2--O--或R''3--CO--O--的基团,其中R'3为烷基、三氟甲基、三氯甲基或被卤素原子或烷基、硝基取代的苯基,R''3定义同R'3或代表被酰基或烷氧羰基取代的甲基,或代表在2位被酰基或烷氧羰基取代的乙基或丙基。这些化合物作为制备抗生素3-硫代乙烯基头孢菌素的中间体具有应用价值。
  • 3-Thiovinyl-cephalosporins
    申请人:Rhone-Poulenc Industries
    公开号:US04307116A1
    公开(公告)日:1981-12-22
    Novel cephalosporins of the general formula (I); ##STR1## in which R is alkyl, L-2-amino-2-carboxy-ethyl, phenyl, pyridyl, pyridyl-N-oxide, pyrimidin-2-yl, substituted pyridazin-3-yl, 5,6-dioxo-1,4,5,6-tetrahydro-1,2,4-triazin-3-yl substituted in the 4-position, 1,3,4-triazol-5-yl or 2-alkoxycarbonyl-1,3,4-triazol-5-yl substituted in the 1-position, 1,4-dialkyl-5,6-dioxo-1,4,5,6-tetrahydro-1,2,4-triazin-3-yl, 1-alkyl-5,6-dioxo-1,4,5,6-tetrahydro-1,2,4-triazin-3-yl, 2-alkyl-5,6-dioxo-1,2,5,6-tetrahydro-1,2,4-triazin-3-yl, triazol-5-yl, 1,3,4-thiadiazol-5-yl which is substituted or unsubstituted, 1,2,4-thiadiazol-5-yl which is substituted, 1,3,4-oxadiazol-5-yl which is substituted or unsubstituted, oxazol-2-yl which is substituted or unsubstituted or tetrazol-5-yl which is substituted or unsubstituted in the 1-position, R' is a hydrogen atom or a radical of the general formula (II); ##STR2## and R.sup.o is hydrogen, alkyl, vinyl or cyanomethyl, as well as their salts, are useful as anti-bacterial agents.
    新型头孢菌素类化合物,其通式为(I);##STR1##其中R为烷基、L-2-氨基-2-羧基乙基、苯基、吡啶基、吡啶基-N-氧化物、嘧啶-2-基、取代的吡啶-3-基、4-位取代的5,6-二氧代-1,4,5,6-四氢-1,2,4-三嗪-3-基、1,3,4-三唑-5-基或1-位取代的2-烷氧羰基-1,3,4-三唑-5-基、1,4-二烷基-5,6-二氧代-1,4,5,6-四氢-1,2,4-三嗪-3-基、1-烷基-5,6-二氧代-1,4,5,6-四氢-1,2,4-三嗪-3-基、2-烷基-5,6-二氧代-1,2,5,6-四氢-1,2,4-三嗪-3-基、三唑-5-基、取代或未取代的1,3,4-噻二唑-5-基、取代的1,2,4-噻二唑-5-基、取代或未取代的1,3,4-噁二唑-5-基、取代或未取代的噁唑-2-基或1-位取代或未取代的四唑-5-基,R'为氢原子或通式(II)的基团;##STR2##且R.sup.o为氢、烷基、乙烯基或氰甲基,以及它们的盐,可用作抗菌剂。
  • 1,2,4-Triazines
    申请人:Rhone-Poulenc Industries
    公开号:US04347359A1
    公开(公告)日:1982-08-31
    New thiols of the general formula: ##STR1## wherein A represents a 2-hydroxy-1-oxoethan-1-yl-2-ylidene or alkoxycarbonylmethyne radical or a nitrogen atom and R represents various substituted alkyl radicals, and their alkali metal and alkaline earth metal salts are useful as intermediates in the preparation of cephalosporins having anti-bacterial properties.
    通式为:##STR1## 其中A代表2-羟基-1-氧代乙基-1-基-2-亚甲基或烷氧羰基亚甲基基团或氮原子,R代表各种取代烷基基团,它们的碱金属和碱土金属盐在制备具有抗菌性能的头孢菌素中起到中间体的作用。
  • Cephalosporin derivatives
    申请人:Rhone-Poulenc Industries
    公开号:US04365062A1
    公开(公告)日:1982-12-21
    New cephalosporins of the formula: ##STR1## in which n=0 or 1, R.sub.1 is a radical of the formula: ##STR2## [in which R.sub.4 is a protective radical and R.sub.5 is hydrogen, alkyl, vinyl, cyanomethyl or a protective radical], or R.sub.1 is a protective radical and R.sub.2 is a protective radical or an enzymatically removable radical, or R.sub.1 is an acyl radical which may be substituted in various ways and R.sub.2 is a protective radical, in the 3-oxoethyl-bicyclooct-2-ene or -bicyclooct-3-ene or 3-oxoethylidene-bicyclooctane form if n=0, and in the 3-oxoethyl-bicyclooct-2-ene or 3-oxoethylidene-bicyclooctane form if n=1, are useful as intermediates for the preparation of 3-thiovinyl-cephalosporins useful as antibacterial agents.
    公式为:##STR1##的新头孢菌素,其中n=0或1,R.sub.1是公式的基团:##STR2## [其中R.sub.4是保护基团,R.sub.5是氢,烷基,乙烯基,氰甲基或保护基团],或R.sub.1是保护基团,R.sub.2是保护基团或酶可去除的基团,或R.sub.1是酰基基团,可以以不同的方式被取代,R.sub.2是保护基团,如果n=0,则为3-氧乙基-双环辛-2-烯或-双环辛-3-烯或3-氧乙基亚双环辛烷形式,如果n=1,则为3-氧乙基-双环辛-2-烯或3-氧乙基亚双环辛烷形式,可用作制备3-硫基乙烯基头孢菌素的中间体,用作抗菌剂。
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