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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973787Generated: October 29, 2026

1,3-Dimethyl-2-imidazolidinone → HCID 11492850, compound

https://huagongshe.com/reaction/973787

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Dimethyl-2-imidazolidinoneHCID 6661—
ReactantSodiumHCID 5360545—
ReactantHCID 14997474HCID 14997474—
ReactantHCID 15811185HCID 15811185—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 11492850HCID 1149285046%

Reaction Conditions

Temperature55 °C

Reaction Steps

To a 15 ml single neck round-bottom flask equipped with magnetic stirrer and under nitrogen atmosphere was added 60 mg (0.484 mmol) of the sodium salt of methyl 3-hydroxyacrylate in 1.5 ml of DMF. The resulting solution was stirred in the presence of 4A molecular sieves overnight and then filtered into another reaction vessel fitted with condenser, nitrogen line and a magnetic stirrer. To the mixture was charged 52 μl (0.467 mmol) N,N'-dimethylimidazolidinone and the solution was heated to 55° C. To this reactor was added a solution of 93 mg (0.388 mmol) of N-cyclopropyl-6,7-difluoro-2H-3, 1-benzoxazine-2,4(1H) dione in 1.5 ml of DMF. The reaction mixture was stirred at 55° C. for 1 hour. The system was allowed to cool to room temperature and was then added to 30 ml of water at pH 4.0. The pH of the resulting suspension was adjusted to 5.5 and the mixture was cooled to 0° C. and filtered. After drying there was obtained 50 mg (46%) of methyl 1-cyclopropyl-6,7-difluoro-1, 4-dihydro-4-oxo-3-quinolinecarboxylate, m.p.: 223° -224° C. The filtrate was extracted with methylene chloride and after drying and evaporation there was obtained an additional 47 mg (43.5%, total yield: 89.5%) of the desired product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05064958
Source datasetuspto-grants-1991_11
ORD IDord-bb15fb46e3f44f9aa6557848ebde4786
Source noteuspto-grants-1991_11