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HRID 720722作成日:2026年10月26日

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

https://huagongshe.com/reaction/720722

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物6-Hydrazinylpyridine-3-sulfonamideHCID 12096590—
反応物N-(1-ethoxy-ethylidene)-3-fluoro-benzamideHCID 21894666—
溶媒MethanolHCID 887—
溶媒DichloromethaneHCID 6344—
生成物6-[5-(3-Fluoro-phenyl)-3-mehtyl-[1,2,4]triazole-1-yl]-pyridine-3-sulfonic acid amideHCID 1019342053.1%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07135572B2
出典データセットuspto-grants-2006_11
ORD IDord-23725d2ef6a84069aac5f17ee02c3ee7
出典メモuspto-grants-2006_11