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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1869289Generated: November 1, 2026

5-Methyl-1,2-oxazole-4-carbonyl chloride → HCID 11739980, compound

https://huagongshe.com/reaction/1869289

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Methyl-1,2-oxazole-4-carbonyl chlorideHCID 2759917—
Reactant1-(3-Amino-5-bromobenzofuran-2-yl)ethanoneHCID 10977986—
SolventWaterHCID 962—
ProductHCID 11739980HCID 11739980—

Reaction Conditions

Temperature27 °C

Reaction Steps

To a solution (10 ml) of 1-(3-amino-5-bromobenzofuran-2-yl)ethanone (0.2 g, 0.79 mmol) in water-free THF was added dropwise a solution (5 ml) of 5-methylisoxazole-4-carbonyl chloride (0.10 g, 0.79 mmol) in water-free THF under a nitrogen gas with vigorous stirring at 26-28° C. over 5 min. The reaction solution was heated at 65° C. for 2 hr. The reaction mixture was cooled to room temperature and the precipitate was collected by filtration. The precipitate was recrystallized from ethyl acetate to give N-(2-acetyl-5-bromobenzofuran-3-yl)-5-methylisoxazole-4-carboxamide as pale-yellow needle crystals (0.19 g, yield 68.0%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07638540B2
Source datasetuspto-grants-2009_12
ORD IDord-900457c554ca4472891ec6ab77c2efab
Source noteuspto-grants-2009_12