돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17992생성일: 2026년 10월 24일

1-Bromo-4-chlorobutane → Methyl 2-(4-chlorobutyl)-6-(3-chloro-4-fluorobenzyl)-4-hydroxy-3,5-dioxo-2,3,5,6,7,8-hexahydro-2,6-naphthyridine-1-carboxylate

https://huagongshe.com/ko/reaction/17992

반응식

참여 물질

역할이름HCID투입량
반응물1-Bromo-4-chlorobutaneHCID 81364—
반응물Methanol, magnesium salt (2:1)HCID 164537—
반응물HCID 178484497HCID 178484497—
용매Dimethyl SulfoxideHCID 679—
용매MethanolHCID 887—
용매Ethyl AcetateHCID 8857—
생성물Methyl 2-(4-chlorobutyl)-6-(3-chloro-4-fluorobenzyl)-4-hydroxy-3,5-dioxo-2,3,5,6,7,8-hexahydro-2,6-naphthyridine-1-carboxylateHCID 66997340—

반응 조건

온도60 °C

반응 단계

A mixture of 6-(3-chloro-4-fluorobenzyl)-3,4-dihydroxy-N,N-dimethyl-5-oxo-5,6,7,8-tetrahydro-2,6-naphthyridine-1-carboxamide (0.80 g, 2.19 mmol) and magnesium methoxide in methanol (10.6 mL, 6-10% methanol solution available from Aldrich) in DMSO (22 mL) was heated at 60° C. for one hour. Methanol was exhaustively removed under vacuum over 45 minutes. The resulting DMSO solution was treated with 1-bromo-4-chlorobutane (1.80 g, 10.50 mmol) and stirred at 60° C. under an atmosphere of nitrogen for one hour. The reaction mixture was diluted with ethyl acetate and washed with dilute hydrochloric acid. The organic extract was washed with 10% aqueous potassium carbonate, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was triturated with diethyl ether. The solid precipitated was collected by filtration to provide the title compound. ES MS M+1=471

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741315B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-15540333baa24a0c9cdcc19e9e0c7790
출처 메모uspto-grants-2010_06