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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720706생성일: 2026년 10월 25일

Water → 4-[5-(4-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide

https://huagongshe.com/reaction/720706

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TriethylamineHCID 8471—
반응물4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
반응물N-(1-ethoxy-ethylidene)-4-chloro-benzamideHCID 21894670—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물4-[5-(4-Chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamideHCID 1017226158%

반응 단계

N-(1-ethoxy-ethylidene)-4-chloro-benzamide 472 mg (2.09 mmol) was dissolved in a mixed solvent of dichloromethane 20 ml and methanol 10 ml, and 4-hydrazinobenzenesulfonamide hydrochloride 515 mg (2.23 mmol) was added to the solution. Then, triethylamine 0.35 ml (2.51 mmol) was slowly added dropwise at room temperature for 10 minutes 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, 4-[5-(4-chloro-phenyl)-3-methyl-[1,2,4]triazole-1-yl]-benzenesulfonamide (423 mg, yield: 58%) was obtained as a solid phase.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135572B2
출처 데이터셋uspto-grants-2006_11
ORD IDord-2fb89ddae253402da3ae0730db67a8b2
출처 메모uspto-grants-2006_11