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HRID 80641作成日:2026年10月23日

Azidomethyl 2,2-dimethylpropanoate → (4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate

https://huagongshe.com/ja/reaction/80641

反応式

関与物質

役割名称HCID仕込み量
反応物Azidomethyl 2,2-dimethylpropanoateHCID 11521126—
反応物Water butanolHCID 22253497—
反応物Sodium AscorbateHCID 23667548—
反応物5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridineHCID 57708431—
触媒Copper SulfateHCID 24462—
溶媒WaterHCID 962—
生成物(4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalateHCID 57708433—

反応手順

To a solution of azidomethyl pivalate (4.26 g, 27.1 mmol) in 1:1 text -butanol water (90 mL total) was added 5-(prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine (5.45 g, 27.1 mmol), sodium ascorbate (1.4 mL of a 1M solution in water) and copper sulfate (1.4 mL of a 1M solution in water). The solution was stirred at room temperature for 72 hours. Water was added and the suspension was extracted with ethyl acetate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to afford the expected product which was used in the next step without further purification. 1H NMR (DMSO-d6): δ 10.07 (1H, s), 8.43-8.41 (2H, m), 8.00 (1H, d, J=8.8 Hz), 7.88 (1H, dd, J=3.2, 8.8 Hz), 6.32 (2H, s), 5.38 (2H, s), 1.08 (9H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846675B2
出典データセットuspto-grants-2014_09
ORD IDord-6cb9a023f229469fa1e8821c6da6f32f
出典メモuspto-grants-2014_09