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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973957Generated: October 25, 2026

Flufenamic Acid → HCID 15678604, compound

https://huagongshe.com/reaction/973957

Reaction equation

Participants

RoleNameHCIDCharge
ReactantFlufenamic AcidHCID 3371—
ReactantThiosemicarbazideHCID 2723789—
SolventPyridineHCID 1049—
SolventTetrahydrofuranHCID 8028—
ProductHCID 15678604HCID 1567860444%

Reaction Steps

N,N'-Carbonyldiimidazole (4.56 g, 27.6 mmol) is added to a room temperature solution of flufenamic acid (5.07 g, 18.0 mmol) in 70 ml of tetrahydrofuran. The clear yellow solution is stirred at room temperature for three hours. The solution is then added via cannula to a suspension of thiosemicarbazide (3.41 g, 37.5 mmol) in 55 ml of pyridine. The suspension is heated at reflux overnight. The clear orange solution is concentrated in vacuo and the residue is partitioned between ethyl acetate and water. The organic layer is washed with water, dried over magnesium sulfate and concentrated. The resulting solid is slurried with a 1:3 mixture of ethyl acetate and hexane. The off-white solid is collected by filtration providing 2.80 g (44%) of 2-[(3-trifluoromethylphenyl)amino]-benzoic acid, 2-(aminothioxomethyl)hydrazide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05066668
Source datasetuspto-grants-1991_11
ORD IDord-fbdefd5d3db34fa6a34cfed71c317fae
Source noteuspto-grants-1991_11