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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 658671생성일: 2026년 10월 24일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물Sodium NitriteHCID 23668193—
반응물1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbohydrazideHCID 57944951—
용매Acetic AcidHCID 176—
생성물1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbonyl azideHCID 5742242594.4%

반응 조건

온도0 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08076491B2
출처 데이터셋uspto-grants-2011_12
ORD IDord-ab745a2f7d144fb4bef5f841fce8e631
출처 메모uspto-grants-2011_12