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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609058Generated: October 31, 2026

Dimethylformamide → HCID 20083103, compound

https://huagongshe.com/reaction/1609058

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
ReactantO-mesitylenesulfonylhydroxylamineHCID 11009332—
ReactantHCID 178469638HCID 178469638—
SolventDichloromethaneHCID 6344—
ProductHCID 20083103HCID 2008310357%

Reaction Steps

10.7 g (32.9 mmol) of ethyl 6,7-difluoro-4-hydroxy-8-acetoxymethylquinoline-3-carboxylate and 14.2 g (65.8 mmol) of anhydrous potassium carbonate were added to 130 ml of N,N-dimethylformamide, and the solution was stirred at room temperature for 4 hours. 14 g (NET 8.97 g, 49 mmol) of mesitylenesulfonylhydroxyamine was dissolved in 100 ml of methylene chloride, and after drying over sodium sulfate, while cooling on ice, this solution was dropped to the previous solution through 20 minutes. Then, the obtained solution was left overnight as it was. To this solution, 100 ml of water was added, and the solution was stirred at room temperature for 1 hour. The solution was extracted with methylene chloride, and the organic layer was washed. After drying over sodium sulfate, the solvent was removed under reduced pressure and ether was added to the crystal residue. The crystals were filtered off and washed with ether to obtain 6.4 g of the subject compound (97) in a 57% yield. The results of the analysis of this compound were as follows:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05399553
Source datasetuspto-grants-1995_03
ORD IDord-ffa029ba46ce4a7295a34f949ee02033
Source noteuspto-grants-1995_03