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HRID 851005作成日:2026年10月26日
Chlorotrimethylsilane → 7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid
https://huagongshe.com/reaction/851005
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 | Methyl chloroformate | HCID 6586 | — |
| 反応物 | 4-Methylmorpholine | HCID 7972 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | N-Acetyl-L-alanine | HCID 88064 | — |
| 反応物 | 7-Amino-4-hydroxyquinoline-3-carboxylic acid | HCID 10262322 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 7-[[2-(Acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid | HCID 13136876 | 62.7% |
反応手順
A mixture of 3.93 g (30 mmol) of N-acetyl-L-alanine, 3.30 ml (30 mmol) of N-methyl morpholine, 2.33 ml (30 mmol) of methyl chloroformate, and 80 ml of acetonitrile is stirred at -10° to -20° for 30 minutes. A mixture of 4.08 g (20 mmol) of 7-amino-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, 8.4 ml (60 mmol) of triethylamine, 7.6 ml (60 mmol) of chlorotrimethylsilane, and 100 ml of dichloromethane is stirred at room temperature for 30 minutes and then cooled to -20°. The cold mixed anhydride is added to the cold silylated quinoline and stirred with cooling for 3 hours and overnight at room temperature. The reaction mixture is evaporated to dryness and the residue is treated with water. The solid is filtered to give 3.98 g of 7-[[2-(acetylamino)-1-oxopropyl]-amino]-1,4-dihydro-4-oxo-3-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-f223e7d94c4c4fdab919dac0959f113f |
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| 出典メモ | uspto-grants-1983_05 |
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