HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 227229Generated: October 30, 2026
Dimethylformamide → HCID 17974869, compound
https://huagongshe.com/reaction/227229
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3-Pyridinecarboxylic acid, 4-(trifluoromethyl)- | HCID 2777549 | — |
| Reactant | HCID 17974866 | HCID 17974866 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 17974869 | HCID 17974869 | 15.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07560456B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-689ef9abdc8440f980336cf9de2323e4 |
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| Source note | uspto-grants-2009_07 |
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