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HRID 851003作成日:2026年10月25日
Chlorotrimethylsilane → 6-[[(1-Acetyl-2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acid
https://huagongshe.com/reaction/851003
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Isobutyl chloroformate | HCID 62365 | — |
| 反応物 | N-Acetyl-L-proline | HCID 66141 | — |
| 反応物 | 6-Amino-4-hydroxyquinoline-3-carboxylic acid | HCID 3281201 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 6-[[(1-Acetyl-2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acid | HCID 70524247 | 62.4% |
反応手順
A mixture of 7.07 g (45 mmol) of N-acetyl-L-proline, 5.85 ml (45 mmol) isobutyl chloroformate, 4.95 ml 45 mmol) N-methyl morpholine, and 90 ml of dichloromethane is stirred at -10° to -20° for 30 minutes. A mixture of 6.13 g (30 mmol) of 6-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 12.6 ml (90 mmol) triethylamine, 11.4 ml (90 mmol) chlorotrimethylsilane, and 150 ml of dichloromethane is stirred at room temperature for 30 minutes and then is cooled to -20°. The cold mixed anhydride solution is added to the cold silylated quinoline and is stirred with cooling for 4 hours and at room temperature ovenight. The reaction mixture is evaporated to dryness and the residue is treated with 1 N hydrochloric acid and the solid is filtered. The solid is digested with ethanol and filtered to give 6.43 g of 6-[[(1-acetyl- 2-pyrrolidinyl)-carbonyl]amino]-1,4-dihydro-4-oxo-quinolinecarboxylic acid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04382089 |
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| 出典データセット | uspto-grants-1983_05 |
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| ORD ID | ord-23759aa6377740ca9a078275182f5948 |
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| 出典メモ | uspto-grants-1983_05 |
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