化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1415935作成日:2026年10月27日
Chloroform → 1-(3-Benzoylamino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid
https://huagongshe.com/reaction/1415935
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Chloroform | HCID 6212 | — |
| 反応物 | Dimethylformamide | HCID 6228 | — |
| 反応物 | Benzoic anhydride | HCID 7167 | — |
| 反応物 | 1-(3-Amino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid | HCID 11089970 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | Diisopropyl Ether | HCID 7914 | — |
| 生成物 | 1-(3-Benzoylamino-4,6-difluorophenyl)-7-chloro-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid | HCID 54394918 | 92.6% |
反応手順
1-(3-amino-4,6-difluorophenyl)-7-chloro-6-fluoro-4-oxo-1,4-dihydro-1,8-naphthyridine-3-carboxylic acid (310 mg) was added to 920 mg of N,N-dimethylformamide together with 220 mg of benzoic anhydride, which was stirred at 70° C. for 2 hours and at 100° C. for 2.5 hours. The reaction solution was combined with 50 ml of chloroform and 150 ml of distilled water. The solution was separated, the chloroform layer was dried over anhydrous magnesium sulfate and concentrated in vacua. Ethanol (6 ml) was added to the residue, which was allowed to stand. The precipitate was collected by filtration and washed with ethanol and then with diisopropyl ether to give 184 mg of the title compound.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05910498 |
|---|
| 出典データセット | uspto-grants-1999_06 |
|---|
| ORD ID | ord-5903198be8b94c9f9f8299525f10c662 |
|---|
| 出典メモ | uspto-grants-1999_06 |
|---|