Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | p-Toluenesulfonic acid | HCID 6101 | — |
| Edukt | 1,1,1-Trimethoxybutane | HCID 123512 | — |
| Edukt | 2-Chloro-4,5-diamino-6-methylpyrimidine | HCID 275295 | — |
| Lösungsmittel | 2-Methoxyethanol | HCID 8019 | — |
| Produkt | HCID 19012212 | HCID 19012212 | 47,1% |
Reaktionsschritte
A mixture of 2-Chloro-4,5-diamino-6-methylpyrimidine (0.80 g, 5.04 mmol), trimethylorthobutyrate (1.2 ml, 7.6 mmol) and p-TsOH (0.08 g) in 2-methoxyethanol (24 ml) was heated in an oil bath at 140° C. for 24 hours. The product was isolated as described in Step 2 of Example 12 and purified by flash chromatography using EtOAc-hexane (1:1) to give the crystalline titled compound (0.5 g, 47%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US05157026 |
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| Quelldatensatz | uspto-grants-1992_10 |
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| ORD ID | ord-889a2aec602c401a8cdf19bffb69e9b2 |
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| Quellennotiz | uspto-grants-1992_10 |
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