HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238819Generated: October 26, 2026
Triethylamine → 2-Amino-4-(2-pyridyl)thiazol-5-yl 2-pyridyl ketone
https://huagongshe.com/reaction/2238819
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Thiourea | HCID 2723790 | — |
| Reactant | 1,3-Di(2-pyridyl)-1,3-propanedione | HCID 2728494 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 2-Amino-4-(2-pyridyl)thiazol-5-yl 2-pyridyl ketone | HCID 23144668 | 51% |
Reaction Steps
1,3-Di(2-pyridyl)propane-1,3-dione (1.17 g, 5.15 mmol) was dissolved in acetic acid (20 mL), and bromine (856 mg, 5.35 mmol) was added thereto, followed by stirring at 80° C. for 1 hour. The reaction mixture was concentrated under reduced pressure, and the resulting residue was suspended in ethanol (30 mL), and triethylamine (0.750 mL, 5.38 mmol) and thiourea (416 mg, 5.47 mmol) were added thereto, followed by stirring under heating and reflux for 30 minutes. Aqueous saturated sodium hydrogencarbonate solution was added to the reaction mixture, followed by extraction with chloroform. The solvent was distilled away under reduced pressure, and the resulting residue was purified through silica gel column chromatography (chloroform:methanol=9:1) to afford the entitled Compound 630 (739 mg, 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07718808B2 |
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| Source dataset | uspto-grants-2010_05 |
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| ORD ID | ord-44b6753e32214b8f94d179881ce9b196 |
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| Source note | uspto-grants-2010_05 |
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