HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1050361Generated: November 2, 2026
Phosphorus sulfide (P2S5) → HCID 118599135, compound
https://huagongshe.com/reaction/1050361
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus sulfide (P2S5) | HCID 14817 | — |
| Reactant | HCID 118598746 | HCID 118598746 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 118599135 | HCID 118599135 | — |
Reaction Steps
A vial was charged with 3-chloro-6-oxo-5-(pyrimidin-4-ylamino)-1,6-dihydropyridine-2-carboxylate (3, 0.35, 1.2 mmol) and pyridine (10 mL) was added. To the above mixture phosphorus pentasulfide (0.53 g, 2.4 mmol) was added and reaction was heated at 110° C. for 16 h. TLC showed presence of starting material and phosphorus pentasulfide (0.265 g, 1.2 mmol) was added again and heated the reaction to 115° C. for 24 h. The pyridine was removed under reduced pressure and water (20 mL) was added and extracted with 5% methanol in dichloromethane (100 mL). The organic layer was washed with sodium bicarbonate and brine and layer was concentrated to dryness to afford ethyl 3-chloro-5-(pyrimidin-4-ylamino)-6-thioxo-1,6-dihydropyridine-2-carboxylate (4) as brownish yellow solid and used directly without further purification. Yield: 350 mg, crude; MS (ESI) m/z 310.94 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382248B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-e611304eb8d7473288991538abab1235 |
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| Source note | uspto-grants-2016_07 |
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