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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1387280생성일: 2026년 10월 25일

1-(4-Methoxybenzyl)-5-iodo-4-methyl-3-nitro-2-pyridone → 3-Amino-1-(4-methoxybenzyl)-5-iodo-4-methyl-2-pyridone

https://huagongshe.com/reaction/1387280

반응식

참여 물질

역할이름HCID투입량
반응물1-(4-Methoxybenzyl)-5-iodo-4-methyl-3-nitro-2-pyridoneHCID 21706516—
용매Acetic AcidHCID 176—
용매Hydrochloric AcidHCID 313—
생성물3-Amino-1-(4-methoxybenzyl)-5-iodo-4-methyl-2-pyridoneHCID 2170647629%

반응 단계

To a stirred solution of 1-(4-methoxybenzyl)-5-iodo-4-methyl-3-nitro-2-pyridone (1.00 g, 2.5 mmol) in acetic acid (12 mL), cooled on ice, was added a solution of stannous chloride dihydrate (2.85 g, 12.6 mmol) in concentrated HCl (8 mL). After 1 hour the mixture was filtered, and the filtrate was neutralized with solid sodium carbonate (adding water as necessary). The mixture was extracted with methylene chloride, and the organic phase was washed, dried, and evaporated to give 3-amino-1-(4-methoxybenzyl)-5-iodo-4-methyl-2-pyridone (0.265 g, 29%) as an oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06268365B1
출처 데이터셋uspto-grants-2001_07
ORD IDord-d39fdad5c40b481891c39949eed13349
출처 메모uspto-grants-2001_07