참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Methyl-2(1H)-pyridinone | HCID 12755 | — |
| 반응물 | Chlorosulfonic acid | HCID 24638 | — |
| 용매 | Water | HCID 962 | — |
| 생성물 | 1-Methyl-6-oxo-1,6-dihydropyridine-3-sulfonic acid, ammonium salt | HCID 131731948 | 48.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08859774B2 |
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| 출처 데이터셋 | uspto-grants-2014_10 |
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| ORD ID | ord-ef170e70f33c4e3fa83ab664e4c0dc3a |
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| 출처 메모 | uspto-grants-2014_10 |
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