CAS: 330944-50-8; (2S,3S)-3-((Z)-2-(2-Aminothiazol-4-yl)-2-(((1-(Tert-Butoxy)-2-Methyl-1-Oxopropan-2-yl)Oxy)Imino)Acetamido)-2-Methyl-4-Oxoazetidine-1-Sulfonic Acid

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    (3S-trans)-3-Amino-4-methyl-2-oxo-1-azetidinesulfonic acid (Z)-2-(2-aminothiazol-4-yl)-2-(1-tert-butoxycarbonyl-1-methylethoxy)iminoacetic acid azthreonam

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    • 80082-65-1 = 330944-50-8
      反应条件:1.1 Reagents: Triethylamine Solvents: Dichloromethane,Water; -10 °C; 15 - 20 H,-10 °C -> 5 °C1.2 Reagents: Hydrochloric Acid Solvents: Water; Ph 1.5 - 2
      标题:A New Process To Synthesize Aztreonam
      作者:Chen,Kai; Zhong,Wei-Hui
      参考文献:Zhejiang Huagong 日期:2013 卷标:44(7) 页码:10-13]

      80082-65-1 + 89604-92-2 = 330944-50-8
      反应条件:1.1 Reagents: Triethylamine Solvents: Tetrahydrofuran,Water; 20 Min,Cooled1.2 20 Min,Cooled; 30 Min,Cooled; 4.5 H,Cooled
      标题:Synthesis Of Aztreonam
      作者:Deng,Qihua; Zhang,Hong; Huang,Wencai
      参考文献:Zhongguo Yiyao Gongye Zazhi 日期:2009 卷标:40(10) 页码:728-730]

      134203-50-2 + 10549-76-5 = 330944-50-8
      反应条件:1.1 Reagents: Triethylamine Solvents: Acetonitrile,Tetrahydrofuran; Rt -> -6 °C; -6 °C; 0.5 H,-6 °C; 4 H,-3 °C1.2 Reagents: Trifluoroacetic Acid Solvents: Tetrahydrofuran; Ph 4.51.3 Reagents: Hydrochloric Acid Solvents: Water; Overnight,Ph 2,2 °C
      标题:Synthesis Of Aztreonam
      作者:Zhang,Qiu; Qiu,Zong-Yin; Lan,Zhi-Yin; Zheng,Jiao-Ni
      参考文献:Zhongguo Xinyao Zazhi 日期:2008 卷标:17(5) 页码:393-395
    📜氨曲南主环,头孢他啶侧链酸活性酯置于三乙胺体系中,用 乙腈,水,乙酸乙酯 用作溶剂,化学反应 0.67H,反应生成氨曲南杂质37
    参考文献: Preparation Of Aztreonam[fr] Preparation D'Aztreonam
    标题: Preparation Of Aztreonam[fr] Preparation D'Aztreonam
    摘要:本发明涉及一种合成阿曲霉素的方法.具体地,该方法包括水解[3S-[3α(Z),4β]]-3-[[(2-氨基-4-噻唑基)[(1-T-叔丁氧羰基-1-甲基乙氧基)亚氨基]乙酰]氨基]-4-甲基-2-氧代-1-氮杂环己烷磺酸(t-Bu阿曲霉素)以形成阿曲霉素.

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    专利信息


    专利号:US-7145017-B2
    优先权日:2002-08-05
    标题 :Preparation of Aztreonam
    发明人:GYOLLAI VIKTOR; MESZAROS SOS ERZSEBET; SZABO CSABA; SINGER CLAUDE; SALYI SZABOLCS
    权利人:TEVA GYOGYSZERGYAR ZARTKOERUEN
    摘要:The invention relates to a process for the synthesis of Aztreonam. Specifically, the process entails hydrolyzing [3S-[3α(Z),4β]]-3-[[(2-amino-4-thiazolyl)[(1-t-butoxycarbonyl-1-methylethoxy)imino]acetyl]amino]-4-methyl-2-oxo-1-azetidinesulfonic acid (t-Bu Aztreonam) to form Aztreonam.

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