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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720722생성일: 2026년 10월 24일

Water → 6-[5-(3-Fluoro-phenyl)-3-mehtyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide

https://huagongshe.com/ko/reaction/720722

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물6-Hydrazinylpyridine-3-sulfonamideHCID 12096590—
반응물N-(1-ethoxy-ethylidene)-3-fluoro-benzamideHCID 21894666—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물6-[5-(3-Fluoro-phenyl)-3-mehtyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amideHCID 1019342053.1%

반응 단계

N-(1-ethoxy-ethylidene)-3-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 collected 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-(3-fluoro-phenyl)-3-mehtyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amide (370 mg, yield: 53%) was obtained as a solid phase.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135572B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-23725d2ef6a84069aac5f17ee02c3ee7
출처 메모uspto-grants-2006_11