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HRID 658671作成日:2026年10月24日

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

https://huagongshe.com/ja/reaction/658671

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US08076491B2
出典データセットuspto-grants-2011_12
ORD IDord-ab745a2f7d144fb4bef5f841fce8e631
出典メモuspto-grants-2011_12