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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227229Generated: October 30, 2026

Dimethylformamide → HCID 17974869, compound

https://huagongshe.com/reaction/227229

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantOxalyl chlorideHCID 65578—
Reactant3-Pyridinecarboxylic acid, 4-(trifluoromethyl)-HCID 2777549—
ReactantHCID 17974866HCID 17974866—
SolventDichloromethaneHCID 6344—
ProductHCID 17974869HCID 1797486915.7%

Reaction Conditions

Temperature20 °C

Reaction Steps

Oxalyl chloride (0.6 ml) was added to a suspension of 4-trifluoromethylnicotinic acid (1 g) and a catalytic amount of N,N-dimethylformamide in dichloromethane, and stirred at 20° C. for 1 hour. 4-Benzyl-5-imino-1,3,4-thiadiazoline hydrobromide (1.44 g) was added under ice cooling, and was stirred at 20° C. for 1 hour. The mixture was then washed (water), dried (magnesium sulfate), evaporated and the residue recrystallized (ethanol) to give 4-benzyl-5-(4-trifluoromethyl-3-pyridylcarbonyl)imino-1,3,4-thiadiazoline (0.3 g, Compound E-39).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07560456B2
Source datasetuspto-grants-2009_07
ORD IDord-689ef9abdc8440f980336cf9de2323e4
Source noteuspto-grants-2009_07