HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 367195Generated: October 29, 2026
Thionyl Chloride → 2-Chloronicotinoyl chloride
https://huagongshe.com/reaction/367195
Participants
| Role | Name | HCID | Charge |
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| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 2-Chloronicotinic acid | HCID 76258 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Chloronicotinoyl chloride | HCID 2774541 | — |
Reaction Steps
A mixture of 3.635 g (23.07 mmol) of 2-chloronicotinic acid, 20 ml of thionyl chloride and three droplets of DMF was heated under reflux for 3 hours. The reaction solution was allowed to cool, and then concentrated under reduced pressure to obtain 2-chloronicotinoyl chloride. The compound thus obtained was then dissolved in 10 ml of acetone. The solution thus obtained was then added dropwise to a solution of 1.931 g of ammonium thiocyanate in 20 ml of acetone with stirring in 5 minutes. After the termination of dropwise addition, the reaction mixture was heated to a temperature of 40° C. with stirring for 5 minutes. The resulting insoluble matters were then removed by filtration to obtain an acetone solution of 2-chloronicotinoyl isothiocyanate. To the solution thus obtained was then added dropwise a solution of 2.171 g of 3-aminopyridine in 20 ml of acetone with stirring for 5 minutes. The reaction mixture was stirred at room temperature for 17 hours, and then poured into about 1,000 ml of ice-water. The resulting crystal was collected by filtration, washed with water, and then dried under reduced pressure to obtain 3.881 g of 1-(2-chloroniconinoyl)-3-(3-pyridyl)thiourea
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06133258 |
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| Source dataset | uspto-grants-2000_10 |
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| ORD ID | ord-b276c366579045aba48bed686763959f |
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| Source note | uspto-grants-2000_10 |
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