Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615332Generated: October 30, 2026

Dimethylformamide → HCID 20427616, compound

https://huagongshe.com/reaction/615332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
Reactant[7-Chloro-3-(ethoxycarbonyl)-6-fluoro-4-oxoquinolin-1(4H)-yl]methanimidic acidHCID 3021289—
ProductHCID 20427616HCID 20427616—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 14.65 g (0.047 mole) of ethyl 7-chloro-6-fluoro-1-(formylamino)-1,4-dihydro-4-oxo-3-quinolinecarboxylate (Preparation 2), 12.9 g (0.094 mole) of potassium carbonate and 200 ml of dimethylformamide was stirred at 25° C. for 90 minutes. Methyl iodide (20.0 g, 0.141 mole) was then added and the reaction mixture was stirred at room temperature for 90 minutes. The dimethylformamide was removed in high vacuum at 50° C., and the residue was partitioned between 250 ml of water and 500 ml of chloroform. The chloroform layer was separated and dried over anhydrous magnesium sulfate. There was obtained from the chloroform solution upon concentration 13.8 g of ethyl 7-chloro-6-fluoro-1,4-dihydro-5-[(formyl)methylamino]-4-oxo-3-quinolinecarboxylate, m.p. 213°-216° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04499091
Source datasetuspto-grants-1985_02
ORD IDord-e95da60994f24d97ad839b4f273b6b29
Source noteuspto-grants-1985_02