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HRID 59046作成日:2026年10月27日
Water → (S)-9-Fluoro-3-Methyl-10-(4-Methylpiperazin-1-yl)-6-(5-oxo-4,5-Dihydro-1H-Tetrazol-1-yl)-2,3-Dihydro-7H-[1,4]Oxazino[2,3,4-IJ]Quinolin-7-One
https://huagongshe.com/reaction/59046
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Water | HCID 962 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Levofloxacin | HCID 149096 | — |
| 反応物 | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | (S)-9-Fluoro-3-Methyl-10-(4-Methylpiperazin-1-yl)-6-(5-oxo-4,5-Dihydro-1H-Tetrazol-1-yl)-2,3-Dihydro-7H-[1,4]Oxazino[2,3,4-IJ]Quinolin-7-One | HCID 137167451 | — |
反応手順
Diphenyl phosphoryl azide (323 μL, 1.5 mmol) was added to a stirred solution of Levofloxacin (361 mg, 1.0 mmol) and Et3N (280 μL, 2.0 mmol) in CH2Cl2 (10 mL) at 0° C. under an atmosphere of nitrogen. The mixture was stirred at 0° C. for 15 min, then allowed to warm to room temperature and stirred for 4 hr. Further aliquots of diphenyl phosphoryl azide (323 μL, 1.0 mmol) and Et3N (280 μL, 2.0 mmol) were added and the mixture was stirred at room temperature overnight. H2O (20 mL) and CH2Cl2 (15 mL) were added and the aqueous and organic layers were partitioned. The aqueous layer was extracted with CH2Cl2 (2×20 mL), and the combined organic layers were dried over Na2SO4, filtered and the solvent was removed under vacuum to leave a crude residue.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09439888B2 |
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| 出典データセット | uspto-grants-2016_09 |
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| ORD ID | ord-97d379b18bcd4bd7bec6fe78254c73ef |
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| 出典メモ | uspto-grants-2016_09 |
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