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HRID 344846作成日:2026年10月25日
Hydrochloric Acid → 8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid
https://huagongshe.com/reaction/344846
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | 8-Chloro-3-ethoxycarbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine | HCID 14700549 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 生成物 | 8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid | HCID 14700554 | 92.4% |
反応手順
A suspension of 8-chloro-3-ethoxycarbonyl-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]-naphthyridine (15 g) in acetic acid (150 cc) and 17.5% strength aqueous hydrochloric acid solution (150 cc) is heated to a temperature in the region of 100° C. with stirring for 4 hours. After cooling to a temperature in the region of 20° C., the product is drained, washed with water (2×100 cc) and washed with ethanol (2×150 cc) and then ethyl ether (2×100 cc). 8-Chloro-7-fluoro-1-methyl-4-oxo-1,4-dihydrobenzo[b][1,8]naphthyridine-3-carboxylic acid (12.7 g) is obtained in the form of a beige solid, subliming at 400°-405° C., which is used without further purification for the subsequent steps.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05053509 |
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| 出典データセット | uspto-grants-1991_10 |
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| ORD ID | ord-2742418d14ba4f89a1e7f076e3f66b8b |
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| 出典メモ | uspto-grants-1991_10 |
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