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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1410126Generated: October 28, 2026

3,5-Dimethyl-4-(tributylstannyl)isoxazole → 5-(3,5-dimethylisoxazol-4-yl)-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile

https://huagongshe.com/reaction/1410126

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,5-Dimethyl-4-(tributylstannyl)isoxazoleHCID 15062215—
Reactant5-iodo-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrileHCID 67120073—
CatalystHCID 178418476HCID 178418476—
Product5-(3,5-dimethylisoxazol-4-yl)-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrileHCID 67120025135.3%

Reaction Steps

5-iodo-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile (450 mg, 1.33 mmol), 3,5-dimethyl-4-(tributylstannyl)isoxazole (907 mg, 2.35 mmol) and PdCl2(PPh3)2 (186 mg, 0.27 mmol), were mixed with 1 mL degassed dioxane and 1 mL degassed DME under nitrogen in a microwave vial. The reaction was run at 145° C. in the microwave for 30 min. Water was added, extracted with CH2Cl2, filtered through a phase separator. The organic phase was evaporated and the residue was purified using silica to give 5-(3,5-dimethylisoxazol-4-yl)-1-(4-methoxyphenyl)-3-methyl-1H-pyrazole-4-carbonitrile (555 mg, >100%) which was used as such in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921402B2
Source datasetuspto-grants-2014_12
ORD IDord-dda3baac04194be3b49e6d492fe9c69f
Source noteuspto-grants-2014_12