Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720717생성일: 2026년 10월 25일
Water → 6-[5-(4-Fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide
https://huagongshe.com/reaction/720717
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | 6-Hydrazinylpyridine-3-sulfonamide | HCID 12096590 | — |
| 반응물 | HCID 21894667 | HCID 21894667 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 6-[5-(4-Fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide | HCID 10172083 | 56.1% |
반응 단계
N-(1-ethoxy-ethylidene)-4-fluoro-benzamide 438 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and 6-hydrazinopyridine-3-sulfonic acid amide 433 mg (2.23 mmol) was added to the solution and stirred for 8 hours. After completing the reaction, water 20 ml was added to the reacting solution and extracted two times with dichloromethane, and then, the organic layer was washed with saturated brine. The organic layer was dried with anhydrous magnesium sulfate, filtered and concentrated under reduced pressure, and the resulting product was re-crystallized in acetone and hexane phase. As a result, 6-[5-(4-fluoro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide (391 mg, yield: 56%) was obtained as a solid phase.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07135572B2 |
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| 출처 데이터셋 | uspto-grants-2006_11 |
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| ORD ID | ord-6115723cc5df4d30b4c912d3b3e37bb6 |
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| 출처 메모 | uspto-grants-2006_11 |
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