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HRID 38752作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物BromoformHCID 5558—
反応物DichloromethaneHCID 6344—
反応物Dichloroacetic AcidHCID 6597—
反応物Sodium NitriteHCID 23668193—
反応物Methyl 2-((5-amino-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetateHCID 59763691—
触媒Benzyl triethylammonium chlorideHCID 66133—
生成物Methyl 2-((5-bromo-4-(4-cyclopropylnaphthalen-1-yl)-4H-1,2,4-triazol-3-yl)thio)acetateHCID 5781144685%

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08524754B2
出典データセットuspto-grants-2013_09
ORD IDord-83895df429f74054be8d620d0aef6216
出典メモuspto-grants-2013_09