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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1370269Generated: November 2, 2026

Dimethylformamide → HCID 18510765, compound

https://huagongshe.com/reaction/1370269

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTriethylamineHCID 8471—
ReactantPyrimidine-5-carboxaldehydeHCID 2761034—
ReactantHCID 13586806HCID 13586806—
ReactantN-(4-Benzoylphenyl)prop-2-enamideHCID 14146482—
SolventPyridineHCID 1049—
ProductHCID 18510765HCID 18510765—

Reaction Conditions

Temperature50 °C

Reaction Steps

1-Chloro-2,4-pyrrolidinedione (0.011 mol; 98%) was added portionwise to a solution of 5-pyrimidinecarboxaldehyde, oxime (0.036 mol) in DMF (50 ml) and this mixture was heated to 50° C. to start the reaction. The mixture was cooled to RT. Pyridine (0.28 ml) was added. The rest of 1-chloro-2,4-pyrrolidinedione (0.043 mol) was added portionwise and the mixture was stirred for 3 hours at RT. N-(4-benzoylphenyl)propenamide (0.025 mol) was added. Triethylamine (0.053 mol) was added dropwise and the resulting reaction mixture was stirred overnight at RT. The crude mixture was washed with water, then extracted with EtOAc. The organic layer was separated, and the solvent was evaporated. The residue was washed with water and extracted with CH2Cl2. The separated organic layer was dried (Na2SO4), filtered and the solvent was evaporated. The residue was crystallized from CH3OH, washed with diethyl ether and hot CH2Cl2, dried and repurified by HPLC over silica gel (eluent: CH2Cl2/CH3OH 97/3). The pure fractions were collected and the solvent was evaporated, yielding 3.5 g of (±)-N-(4-benzoylphenyl)-4,5-dihydro-3-(5-pyrimidinyl)-5-isoxazolecarboxamide (compound 349)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06583141B1
Source datasetuspto-grants-2003_06
ORD IDord-34905012734f4411a6a91b4ace8eadb3
Source noteuspto-grants-2003_06