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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 420068Generated: October 30, 2026

Oxalyl chloride → N-(6-acetyl-2-chloro-3-methoxyphenyl)-5-isopropylisoxazole-3-carboxamide

https://huagongshe.com/reaction/420068

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(Propan-2-yl)-1,2-oxazole-3-carboxylic acidHCID 6483812—
Reactant1-(2-Amino-3-chloro-4-methoxyphenyl)ethanoneHCID 29919988—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
ProductN-(6-acetyl-2-chloro-3-methoxyphenyl)-5-isopropylisoxazole-3-carboxamideHCID 6665063760%

Reaction Steps

To a stirred solution of 5-isopropylisoxazole-3-carboxylic acid (3.5 g, 22.6 mmol) in DCM (35 mL) was added anhydrous DMF (few drops) and oxalyl chloride (3.82 mL, 43.2 mmol) at 0° C. under nitrogen. At the end of the gas escape, the reaction mixture was allowed to warm up to room temperature. The mixture was stirred at room temperature for 2 hrs and was evaporated. Dioxane (70 mL) was added under nitrogen, followed by a solution of 1-(2-amino-3-chloro-4-methoxy-phenyl)-ethanone 40d (4.10 g, 20.6 mmol) in dioxane (15 mL). The reaction mixture was stirred at room temperature for 16 hrs. NaHCO3 was then added. The mixture was extracted with EtOAc. Organics were dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude material was triturated in Et2O to yield compound 92d as a brown solid in 60% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093379B2
Source datasetuspto-grants-2012_01
ORD IDord-c1788423d3bc4795b45a538e82e4ca7e
Source noteuspto-grants-2012_01