돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1589570생성일: 2026년 10월 26일

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

반응식

참여 물질

역할이름HCID투입량
반응물IodoethaneHCID 6340—
반응물TriethylamineHCID 8471—
반응물7-(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—
용매DimethylformamideHCID 6228—
생성물1-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%

반응 단계

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°.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04571396
출처 데이터셋uspto-grants-1986_02
ORD IDord-dee1b1e77f69402284755a2f421b158e
출처 메모uspto-grants-1986_02