戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 386040作成日:2026年10月25日

Methyl propiolate → Methyl 1-[(6-bromopyridin-2-yl)methyl]-1H-1,2,3-triazole-4-carboxylate

https://huagongshe.com/reaction/386040

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl propiolateHCID 13536—
反応物Sodium AscorbateHCID 23667548—
反応物2-(Azidomethyl)-6-bromopyridineHCID 45357403—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
溶媒Sodium BicarbonateHCID 516892—
生成物Methyl 1-[(6-bromopyridin-2-yl)methyl]-1H-1,2,3-triazole-4-carboxylateHCID 58335253—

反応手順

Methyl propiolate (641 μL, 7.63 mmol) and 2-(azidomethyl)-6-bromopyridine (1.25 g, 5.87 mmol) were combined in t-BuOH (9.0 mL) and water (5.0 mL). A solution of CuSO4.5H2O (73 mg, 0.29 mmol) in water (2.0 mL) was added, followed by sodium ascorbate (232 mg, 1.17 mmol) in water (2.0 mL). The reaction was stirred at room temperature for 18 h, during which time it became a yellow suspension. The suspension was diluted with saturated NaHCO3 and extracted with EtOAc (3×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure. The crude solid was purified by flash chromatography (40-100% EtOAc/hexanes) to afford the title compound as a colorless solid.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367706B2
出典データセットuspto-grants-2013_02
ORD IDord-77188be22dc445c88ffeda7909befadf
出典メモuspto-grants-2013_02