参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 反应物 | 1-(1,1-Dimethyl-1-butyloxycarbonyloxy)ethyl chloride | HCID 23449137 | — |
| 反应物 | HCID 23669370 | HCID 23669370 | — |
| 催化剂 | Silver iodide | HCID 24563 | — |
| 溶剂 | N,N-二甲基甲酰胺 | HCID 6228 | — |
| 产物 | HCID 23387834 | HCID 23387834 | 29.9% |
反应步骤
A solution of 156.6 mg of 1-(1,1-dimethyl-1-butyloxycarbonyloxy)ethyl chloride in 2.0 ml of DMF was added to a suspension of 176.1 mg of silver iodide in 2.0 ml of DMF. The mixture was stirred in an argon atmosphere at room temperature for one hr. A solution of 200.0 mg of sodium(1S,5R,6S)-6-((1R)-1-hydroxyethyl)-1-methyl-2-(7-methylthio-imidazo[5,1-b]thiazol-2-yl)-1-carbapen-2-em-3-carboxylate in 1.0 ml of DMF was added thereto, followed by stirring for 3 hr. Water (10 ml) was added to the reaction solution to terminate the reaction. The system was extracted three times with 10 ml of ethyl acetate, followed by washing three times with 30 ml of semisaturated brine. The organic layer was dried over anhydrous magnesium sulfate and filtered. The residue was purified by chromatography on silica gel (chloroform:methanol=20:1) to give 82.3 mg of the title compound.
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US06458780B1 |
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| 来源数据集 | uspto-grants-2002_10 |
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| ORD ID | ord-675901b43e19495ab0dd9350190c3749 |
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| 来源说明 | uspto-grants-2002_10 |
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