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【结 构 式】 
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【分子编号】32620 【品名】3-[2-[(2R,4S)-1-[(allyloxy)carbonyl]-4-([(4R,5S,6S)-2-[(allyloxy)carbonyl]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl]sulfanyl)pyrrolidinyl]ethyl]-1-methyl-1H-imidazol-3-ium iodide 【CA登记号】 |
【 分 子 式 】C27H37IN4O6S 【 分 子 量 】672.58461 【元素组成】C 48.22% H 5.54% I 18.87% N 8.33% O 14.27% S 4.77% |
合成路线1
该中间体在本合成路线中的序号：(XVIII)Cyclization of diazo azetidinone (XIII) by means rhodium(II) octanoate dimer produced the azabicyclo ketone (XIV), which was converted to the phosphorylated carbapenem (XV) employing diphenylphosphorochloridate. Hydrolysis of the thioacetate ester (XII) with NaOMe gave the intermediate thiol (XVI), which was condensed with phosphate (XV) to yield the (pyrrolidinylthio)carbapenem (XVII). Quaternization of the imidazole nucleus of (XVII) with methyl iodide afforded imidazolium salt (XVIII). Then, both allyl ester and allyloxycarbonyl groups of (XVIII) were deprotected using tributyltin hydride and a palladium catalyst. Finally, the iodide salt was exchanged for the corresponding chloride employing an ion exchange resin.
| 【1】 Barrett, D.; Azami, H.; Matsuda, K.; et al.; Synthesis and antibacterial activity of novel 4-pyrrolidinylthio carbapenems. Part III: Novel 2-alkyl substituents containing cationic heteroaromatics linked via a C-N bond. Bioorg Med Chem 1999, 7, 8, 1665. |
| 【2】 Murata, M.; Tsutsumi, H.; Matsuda, K.; Hattori, K.; Nakajima, T. (Fujisawa Pharmaceutical Co., Ltd.); Substd. 3-pyrrolidinylthio-carbapenems as antimicrobial agents. EP 0636133; JP 1995505650; WO 9321186 . |
| 中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
|---|---|---|---|---|---|---|
| (XII) | 32614 | allyl (2R,4S)-4-(acetylsulfanyl)-2-[2-(1H-imidazol-1-yl)ethyl]-1-pyrrolidinecarboxylate | C15H21N3O3S | 详情 | 详情 | |
| (XIII) | 32615 | (4R)-1-(allyloxy)-4-[(2R,3S)-3-[(1R)-1-hydroxyethyl]-4-oxoazetidinyl]-1,3-dioxo-2-pentanediazonium | C13H18N3O5 | 详情 | 详情 | |
| (XIV) | 32616 | allyl (4R,5R,6S)-6-[(1R)-1-hydroxyethyl]-4-methyl-3,7-dioxo-1-azabicyclo[3.2.0]heptane-2-carboxylate | C13H17NO5 | 详情 | 详情 | |
| (XV) | 32617 | allyl (4R,5R,6S)-3-[(diphenoxyphosphoryl)oxy]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate | C25H26NO8P | 详情 | 详情 | |
| (XVI) | 32618 | allyl (2R,4S)-2-[2-(1H-imidazol-1-yl)ethyl]-4-sulfanyl-1-pyrrolidinecarboxylate | C13H19N3O2S | 详情 | 详情 | |
| (XVII) | 32619 | allyl (4R,5S,6S)-3-([(3S,5R)-1-[(allyloxy)carbonyl]-5-[2-(1H-imidazol-1-yl)ethyl]pyrrolidinyl]sulfanyl)-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylate | C26H34N4O6S | 详情 | 详情 | |
| (XVIII) | 32620 | 3-[2-[(2R,4S)-1-[(allyloxy)carbonyl]-4-([(4R,5S,6S)-2-[(allyloxy)carbonyl]-6-[(1R)-1-hydroxyethyl]-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-en-3-yl]sulfanyl)pyrrolidinyl]ethyl]-1-methyl-1H-imidazol-3-ium iodide | C27H37IN4O6S | 详情 | 详情 |