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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 548105Generated: October 25, 2026

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

https://huagongshe.com/reaction/548105

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium NitriteHCID 23668193—
Reactant1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbohydrazideHCID 57944951—
SolventAcetic AcidHCID 176—
Product1-((3,5-dimethylisoxazol-4-yl)methyl)-1H-pyrazole-4-carbonyl azideHCID 5742242594.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07939671B2
Source datasetuspto-grants-2011_05
ORD IDord-b6780e4554bd46c19262727687a6aa61
Source noteuspto-grants-2011_05