HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 973957Generated: October 25, 2026
Flufenamic Acid → HCID 15678604, compound
https://huagongshe.com/reaction/973957
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Flufenamic Acid | HCID 3371 | — |
| Reactant | Thiosemicarbazide | HCID 2723789 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 15678604 | HCID 15678604 | 44% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05066668 |
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| Source dataset | uspto-grants-1991_11 |
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| ORD ID | ord-fbdefd5d3db34fa6a34cfed71c317fae |
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| Source note | uspto-grants-1991_11 |
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