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HRID 2094952作成日:2026年10月26日

Sodium Nitrite → 1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbonyl azide

https://huagongshe.com/reaction/2094952

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium NitriteHCID 23668193—
反応物1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbohydrazideHCID 57944951—
溶媒Acetic AcidHCID 176—
生成物1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbonyl azideHCID 5742242594.4%

反応条件

温度0 °C

反応手順

Sodium nitrite (450 mg, 6.5 mmol, in H2O) (10 mL) was added dropwise, over 10 minutes, to a suspension of 1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbohydrazide (example 10-1b) (1 g, 4.3 mmol) in 10% aqueous acetic acid (50 mL) and cooled to 0° C. via an ice water bath. The reaction was stirred for an additional 15 minutes then extracted with ethyl acetate (3×, 75 mL). The combined organic extracts were washed with aqueous saturated sodium carbonate (100 mL) followed by H2O (100 mL). The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The solid product was triturated with ethyl acetate/hexanes (1/9) and dried en vacuo to afford 1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbonyl azide (1 g, 93%) as a white solid. 1H NMR (CDCl3, 400 MHz): δ2.20 (s, 3H), 2.44 (s, 3H), 5.07 (s, 2H), 7.81 (s, 1H), 7.93 (s, 1H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08445692B2
出典データセットuspto-grants-2013_05
ORD IDord-0de395f19dd0489097335e19b818a320
出典メモuspto-grants-2013_05