HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814239Generated: October 30, 2026
Ethyl oxoacetate → 2,4-Bis[[(2,3-difluorophenyl)methyl]thio]-7(8h)-pteridinone
https://huagongshe.com/reaction/1814239
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl oxoacetate | HCID 70211 | — |
| Reactant | 1-(Bromomethyl)-2,3-difluoro-benzene | HCID 517984 | — |
| Reactant | Sodium | HCID 5360545 | — |
| Reactant | HCID 178509065 | HCID 178509065 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 2,4-Bis[[(2,3-difluorophenyl)methyl]thio]-7(8h)-pteridinone | HCID 22506012 | — |
Reaction Steps
Sodium (3.96 g) was dissolved in methanol (150 ml), 5,6-diamino-2,4-pyrimidinedithiol (15 g) was added, then 2,3-difluorobenzylbromide (30.9 g) slowly added and the reaction mixture was stirred at room temperature under nitrogen for 10 min. Ethyl glyoxalate (15 ml) was added followed by more sodium (2.5 g) and the reaction was left for a further 20 min. The reaction was then quenched with acetic acid (10 ml) and poured on to water (600 ml) with stirring. The resulting precipitate was filtered through celite and washed with water. The filtrate was discarded and the solid was washed through the celite using acetone. The solution was then evaporated to dryness and purified by silica gel column chromatography using 10% ethyl acetate in DCM to yield the sub-titled compound as a cream solid (8 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06875868B2 |
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| Source dataset | uspto-grants-2005_04 |
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| ORD ID | ord-45486d3bdec14dd39efd99888d4d42a8 |
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| Source note | uspto-grants-2005_04 |
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