Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 447809생성일: 2026년 10월 25일
Potassium Carbonate → 5-Chloro-2-imino-1-[3-(dimethylsulfamoyl)benzyl]-1,2-dihydropyridine-3-carboxamide hydrochloride
https://huagongshe.com/reaction/447809
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-Cyano-2-(3,4-dichloro-5(2H)-oxo-2-furyl)acetamide | HCID 541792 | — |
| 반응물 | 3-(Aminomethyl)-N,N-dimethylbenzenesulfonamide | HCID 16795356 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 5-Chloro-2-imino-1-[3-(dimethylsulfamoyl)benzyl]-1,2-dihydropyridine-3-carboxamide hydrochloride | HCID 66969900 | 48.6% |
반응 단계
(Step 2) To a suspension of 2-cyano-2-(3,4-dichloro-5-oxo-2,5-dihydrofuran-2-yl)acetamide (0.73 g) and 3-(aminomethyl)-N,N-dimethylbenzenesulfonamide obtained in Step 1 (1.0 g) in ethanol (10 ml) was added potassium carbonate (0.65 g) at room temperature, and the mixture was stirred overnight at 70° C. The reaction solution was filtered through celite. The solvent was evaporated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:hexane=7:3→1:0). 4N Hydrochloride-ethyl acetate solution (1 ml) was added to the obtained yellow oil, and the precipitated crystals were collected by filtration, and recrystallized to give the title compound (306 mg).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08481569B2 |
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| 출처 데이터셋 | uspto-grants-2013_07 |
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| ORD ID | ord-98c41bf1a73c4337898bd81d5f263ce2 |
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| 출처 메모 | uspto-grants-2013_07 |
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