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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1026615Generated: November 2, 2026

Dimethylformamide → HCID 86668146, compound

https://huagongshe.com/reaction/1026615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 67106662HCID 67106662—
SolventDichloromethaneHCID 6344—
ProductHCID 86668146HCID 8666814692.2%

Reaction Conditions

Temperature0 °C

Reaction Steps

To anhydrous dichloromethane (30 mL) was added oxalyl chloride (0.03 mL, 0.36 mmol). N,N-dimethylformamide (0.03 mL, 0.36 mmol) was added at 0° C., which was then stirred for 30 min at 0° C. To this solution was added 1-(1-isopropylindol-5-yl)-imidazole-4-carboxylic acid ethyl ester (0.09 g, 0.3 mmol) obtained in Preparation 27, and the mixture was stirred for 1 h at room temperature. The solvent was removed, tetrahydrofuran (30 mL) and 20% aqueous ammonium acetate solution (30 mL) were added to the residue, and the mixture was heated for 30 min while being stirred under reflux. The reaction solution was cooled, ethyl acetate was added, and washed with aqueous sodium bicarbonate solution. The organic layer was dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The resulting solid was filtered, washed with ethyl acetate and dried to give the title compound (0.09 g, 92% Yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729273B2
Source datasetuspto-grants-2014_05
ORD IDord-d0b0b4f4019f42fbaabf8633841ce9e3
Source noteuspto-grants-2014_05