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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1257158생성일: 2026년 10월 27일

1-(4-methoxyphenyl)-N-methylmethanamine → 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2,4-difluorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-one

https://huagongshe.com/reaction/1257158

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-methoxyphenyl)-N-methylmethanamineHCID 485407—
반응물3-(5-Amino-2,4-difluorophenyl)-7-chloro-1-methyl-1,6-naphthyridin-2(1H)-oneHCID 86620158—
생성물7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2,4-difluorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-oneHCID 6909649691%

반응 조건

온도200 °C

반응 단계

3-(5-Amino-2,4-difluorophenyl)-7-chloro-1-methyl-1,6-naphthyridin-2(1H)-one (2.4 g, 7.5 mmol) and 4-methoxy-N-methylbenzylamine (10 mL) were combined in a sealed vessel and heated to 200° C. overnight. The volatiles were removed in vacuo and the residue was purified by column chromatography to give 7-((4-methoxybenzyl)(methyl)amino)-3-(5-amino-2,4-difluorophenyl)-1-methyl-1,6-naphthyridin-2(1H)-one (3 g, 91% yield), which was used in the next step without further purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08461179B1
출처 데이터셋uspto-grants-2013_06
ORD IDord-afd6aea872c24105b68e1c8703d7b839
출처 메모uspto-grants-2013_06