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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1801571Generated: October 25, 2026

Diisopropylethylamine → N-(2-chloro-5-formylphenyl)-5-methylisoxazole-3-carboxamide

https://huagongshe.com/reaction/1801571

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Amino-4-chlorobenzaldehydeHCID 245303—
Reactant5-Methylisoxazole-3-carbonyl chlorideHCID 2736894—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN-(2-chloro-5-formylphenyl)-5-methylisoxazole-3-carboxamideHCID 5980318225.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a solution of 3-amino-4-chlorobenzaldehyde 2 (0.267 g, 1.72 mmol) in DCM (5 mL) at 0° C. was added N-ethyl-N-isopropylpropan-2-amine (0.600 mL, 3.44 mmol) and 5-methylisoxazole-3-carbonyl chloride (0.292 g, 2.01 mmol). The reaction mixture was stirred at 0° C. for 30 min, warmed to room temperature, stirred for 1 h, and diluted with EtOAc. The organic phase was washed with saturated NaHCO3 (1×), brine (1×), dried over MgSO4, filtered, and concentrated in vacuo. Purification by flash column chromatography on silica gel (eluted with 15% to 50% EtOAc in hexanes) gave N-(2-chloro-5-formylphenyl)-5-methylisoxazole-3-carboxamide 3 (0.117 g, 25.8% yield) as a white solid. Mass spectrum: calculated for C12H9ClN2O3 264.0. found 265.0 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08349831B2
Source datasetuspto-grants-2013_01
ORD IDord-97b7ab958b164becbed46e3827144cf0
Source noteuspto-grants-2013_01