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HRID 248464作成日:2026年10月26日
7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid → 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(phenoxymethyl)-1-piperazinyl]-3-quinolinecarboxylic acid
https://huagongshe.com/reaction/248464
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 7-Chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid | HCID 483169 | — |
| 反応物 | 3-Phenoxymethylpiperazine | HCID 19763604 | — |
| 溶媒 | Pyridine | HCID 1049 | — |
| 生成物 | 1-Ethyl-6-fluoro-1,4-dihydro-4-oxo-7-[3-(phenoxymethyl)-1-piperazinyl]-3-quinolinecarboxylic acid | HCID 14839355 | 46.9% |
反応手順
A mixture of 2 g of 3-phenoxymethylpiperazine and 701 mg of 7-chloro-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid in 10 ml of pyridine was heated under argon in a pressure bottle at 130° C. for 18 hours. The solvents were removed and the residue chromatographed on silica gel, eluting with chloroform:methanol (9:1). The appropriate fractions were combined, evaporated, triturated with methanol and ether, then dried, giving 519 mg of the desired compound, mp 198°-200° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US05210193 |
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| 出典データセット | uspto-grants-1993_05 |
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| ORD ID | ord-b8fee752830b4340872bb1e8ffe1ea49 |
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| 出典メモ | uspto-grants-1993_05 |
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