HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 648569Generated: October 29, 2026
Potassium Carbonate → HCID 20145030, compound
https://huagongshe.com/reaction/648569
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Sulfuryl chloride | HCID 24648 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | Ethyl α,γ-dioxo-3-pyridinebutanoate | HCID 12246594 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 20145030 | HCID 20145030 | 16.2% |
Reaction Steps
A solution of sulfuryl chloride (2.84 g) in methylene chloride (5 ml) was dropwise added to a solution of ethyl 4-(3-pyridyl)-2,4-dioxo-butyrate (4.42 g) in methylene chloride (40 ml) at 18° C. to 30° C. After being stirred at ambient temperature for one hour, the mixture was added to a solution of thiourea (4.56 g) in a mixture of tetrahydrofuran (50 ml) and water (10 ml). The resulting mixture was adjusted to pH 7.5 with 20% aqueous potassium carbonate and stirred for one hour, and then the solvent was removed in vacuo. To the residue was added a mixture of water and ethyl acetate, and the mixture was acidified to pH 1.0 with 10% hydrochloric acid. The separated aqueous layer was adjusted to pH 9.0 with 20% aqueous potassium carbonate and extracted with ethyl acetate. The extract was dried over magnesium sulfate and evaporated in vacuo. The residue was recrystallized from a mixture of ethyl acetate and tetrahydrofuran to give ethyl 2-amino-5-nicotinoyl-4-thiazolecarboxylate (0.9 g). mp 221° C. (dec.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04735957 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-2921aed18cb242f0a16350c64ab0eecf |
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| Source note | uspto-grants-1988_04 |
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