HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 387214Generated: October 30, 2026
Ethyl Bromide → 6-Bromo-8-ethyl-2-methylsulfanylpyrido[2,3-d]pyrimidin-7-one
https://huagongshe.com/reaction/387214
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-bromo-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one | HCID 22134720 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-8-ethyl-2-methylsulfanylpyrido[2,3-d]pyrimidin-7-one | HCID 66760344 | 76% |
Reaction Steps
To a suspension of NaH (60%, 0.15 g, 3.75 mmol) in anhydrous dimethylformamide (10 mL) was added 6-bromo-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one (2, 0.68 g, 2.50 mmol) at room temperature and the reaction was stirred at 50° C. for 0.5 h. The reaction mixture was cooled to room temperature, ethyl bromide (0.22 mL, 0.32 g, 2.93 mmol) was added, and the reaction was stirred at 50° C. for 1.5 h. The mixture was poured into ice water (10 g), and the white precipitate was collected to give 6-bromo-8-ethyl-2-(methylthio)pyrido[2,3-d]pyrimidin-7(8H)-one (3, 0.57 g, 1.90 mmol, 76%). ESMS m/z 300 (M+H)+. The material was used without any further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08372970B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-b8b663a55a70489282554f7cdc3b33ff |
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| Source note | uspto-grants-2013_02 |
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