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【结 构 式】 
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【分子编号】67100 【品名】4-nitrobenzyl 2-diazo-4-(3-(1-hydroxyethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate 【CA登记号】 |
【 分 子 式 】C17H18N4O7 【 分 子 量 】390.35268 【元素组成】C 52.31% H 4.65% N 14.35% O 28.69% |
与该中间体有关的原料药合成路线共 1 条
合成路线1
该中间体在本合成路线中的序号：(I)
| 【1】 Kanamoto K.2007. Process for producing carbapenem derivatives through reactions without isolating intermediates. WO 2007020960 A1. |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (I) | 67100 | 4-nitrobenzyl 2-diazo-4-(3-(1-hydroxyethyl)-4-oxoazetidin-2-yl)-3-oxopentanoate | C17H18N4O7 | 详情 | 详情 | |
| (II) | 37720 | 4-nitrobenzyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate | C17H18N2O7 | 详情 | 详情 | |
| (III) | 16075 | 4-methoxybenzyl (4R,5R,6S)-3-[(diphenoxyphosphoryl)oxy]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate | C30H30NO9P | 详情 | 详情 | |
| (IV) | 67099 | 4-nitrobenzyl 4-mercapto-2-((sulfamoylamino)methyl)pyrrolidine-1-carboxylate | C13H18N4O6S2 | 详情 | 详情 | |
| (V) | 67098 | nitro(phenyl)methyl 6-(1-hydroxyethyl)-4-methyl-3-((1-(((4-nitrobenzyl)oxy)carbonyl)-5-(((((4-nitrobenzyl)oxy)carbonyl)(sulfamoyl)amino)methyl)pyrrolidin-3-yl)thio)-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate | C38H39N7O16S2 | 详情 | 详情 |
Extended Information