Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 2-Amino-4,6-dichloropyrimidine-5-carboxaldehyde | HCID 265546 | — |
| Reactant | HCID 178418507 | HCID 178418507 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59311385 | HCID 59311385 | 49% |
Reaction Steps
2-Amino-4,6-dichloropyrimidine-5-carbaldehyde (100 g) was suspended in tetrahydrofuran (4000 ml), and a 1 N solution of vinylmagnesium bromide in tetrahydrofuran (2200 g) was added dropwise under ice-cooling. After completion of the dropwise addition, the mixture was stirred under ice-cooling for two hours. Water (2000 ml) was added to the reaction solution, and the solution was made acidic with a 1 N hydrochloric acid solution (2500 ml), followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate and filtered, followed by concentration. Methanol was added to the resulting residue, followed by stirring for one hour. The insoluble matter was filtered off, and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (ethyl acetate-chloroform) to obtain the title compound (50 g, 49%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158638B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-06c0bf9ed94e4a92b579485c47e72460 |
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| Source note | uspto-grants-2012_04 |
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