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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 537263생성일: 2026년 10월 23일

1-Methyl-2(1H)-pyridinone → 1-Methyl-6-oxo-1,6-dihydropyridine-3-sulfonic acid, ammonium salt

https://huagongshe.com/ko/reaction/537263

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참여 물질

역할이름HCID투입량
반응물1-Methyl-2(1H)-pyridinoneHCID 12755—
반응물Chlorosulfonic acidHCID 24638—
용매WaterHCID 962—
생성물1-Methyl-6-oxo-1,6-dihydropyridine-3-sulfonic acid, ammonium saltHCID 13173194848.3%

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온도50 °C

반응 단계

Chlorosulphonic acid (2 ml, 30.1 mmol) was added cautiously dropwise by pipette over 5 minutes to stirred neat 1-methylpyridin-2(1H)-one (8.09 ml, 82 mmol) and the resulting viscous solution was stirred at 50° C. for 40 hours. The cooled solidified reaction mixture was then added cautiously to water (100 ml), giving a clear brown solution. This solution was concentrated in vacuo to 40 ml, then made basic with concentrated ammonia solution, and washed with dichloromethane (6×100 ml). The aqueous phase was then evaporated to give a brown slurry which was triturated in methanol and filtered. The filtrate was evaporated to give 1-methyl-6-oxo-1,6-dihydropyridine-3-sulfonic acid, ammonium salt (3 g) as a brown solid. LCMS (Method F, ES-API): RT 0.46 min, m−H=188.0.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08859774B2
출처 데이터셋uspto-grants-2014_10
ORD IDord-ef170e70f33c4e3fa83ab664e4c0dc3a
출처 메모uspto-grants-2014_10