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HRID 386062作成日:2026年10月27日

Acetic acid, azido-, ethyl ester → ethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetate

https://huagongshe.com/reaction/386062

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic acid, azido-, ethyl esterHCID 69480—
反応物2-Bromo-6-ethynylpyridineHCID 12970532—
反応物Sodium AscorbateHCID 23667548—
溶媒WaterHCID 962—
溶媒tert-ButanolHCID 6386—
溶媒Sodium BicarbonateHCID 516892—
生成物ethyl[4-(6-bromopyridin-2-yl)-1H-1,2,3-triazol-1-yl]acetateHCID 59525977—

反応手順

2-Bromo-6-ethynylpyridine (Example 465, Step 1) (350 mg, 1.92 mmol) and ethyl azidoacetate (1.08 ml, 1.92 mmol) were combined in t-BuOH (4.0 mL) and water (2.0 mL). CuSO4.5H2O (24 mg, 0.096 mmol) in water (1.0 mL) was added, followed by sodium ascorbate (76 mg, 0.39 mmol) in water (1.0 mL). The reaction was stirred at room temperature for 5 h, diluted with saturated NaHCO3, and extracted with EtOAc (2×). The combined organic layers were washed with brine, dried (MgSO4), filtered, and evaporated to a yellow residue that was purified by flash chromatography (0-30% 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-c07ac8fa129843fba3c3213505dc47fb
出典メモuspto-grants-2013_02