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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38752생성일: 2026년 10월 24일

Bromoform → Methyl 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetate

https://huagongshe.com/ko/reaction/38752

반응식

참여 물질

역할이름HCID투입량
반응물BromoformHCID 5558—
반응물DichloromethaneHCID 6344—
반응물Dichloroacetic AcidHCID 6597—
반응물Sodium NitriteHCID 23668193—
반응물Methyl 2-((5-amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetateHCID 59763691—
촉매Benzyl triethylammonium chlorideHCID 66133—
생성물Methyl 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetateHCID 5781144685%

반응 단계

Sodium nitrite (2.76 g, 40 mmol) was added to a solution of methyl 2-(5-amino-4-(1-cyclopropylnaphthalen-4-yl)-4H-1,2,4-triazol-3-ylthio)acetate (0.71 g, 2 mmol) and benzyltriethylammonium chloride (1.63 g, 6 mmol) in bromoform (10 mL). Dichloroacetic acid (0.33 mL, 4 mmol) was then added and the reaction mixture stirred at room temperature for 3 h. The mixture was directly loaded onto a 7-inch column of silica gel, packed with dichloromethane (DCM). The column was first eluted with DCM until all bromoform eluted, then eluted with acetone/DCM (5:95) to give methyl 2-(5-bromo-4-(1-cyclopropylnaphthalen-4-yl)-4H-1,2,4-triazol-3-ylthio)acetate (713 mg, 85%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524754B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-83895df429f74054be8d620d0aef6216
출처 메모uspto-grants-2013_09