戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1589570作成日:2026年10月27日

Iodoethane → 1-Ethyl-7-(5-ethyl-2,5-diazabicyclo[2.2.2]-oct-2-yl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, hydroiodide

https://huagongshe.com/reaction/1589570

反応式

関与物質

役割名称HCID仕込み量
反応物IodoethaneHCID 6340—
反応物TriethylamineHCID 8471—
反応物7-(2,5-Diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acidHCID 13565797—
溶媒DimethylformamideHCID 6228—
生成物1-Ethyl-7-(5-ethyl-2,5-diazabicyclo[2.2.2]-oct-2-yl)-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, hydroiodideHCID 13171452357.7%

反応手順

A solution of 0.35 g (1.0 mmole) of 7-(2,5-diazabicyclo[2.2.2]oct-2-yl)-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-1,8-naphthyridine-3-carboxylic acid, 0.32 ml (4.0 mmole) of ethyl iodide, 0.56 ml (4.0 mmole) triethylamine and 10 ml of N, N-dimethylformamide was heated at 100° for 17 hours. The reaction mixture was evaporated to dryness and the residue was stirred with 25 ml of 1 N sodium hydroxide for one hour. The solution was neutralized to pH 7 with 1 N hydrochloric acid, filtered and evaporated the filtrate to dryness. The residue was recrystallized from ethanol to give 0.29 g of the title compound, mp>300°.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04571396
出典データセットuspto-grants-1986_02
ORD IDord-dee1b1e77f69402284755a2f421b158e
出典メモuspto-grants-1986_02