Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Nitric Acid | HCID 944 | — |
| Edukt | Trifluoroacetic acid | HCID 6422 | — |
| Edukt | HCID 178503559 | HCID 178503559 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | HCID 178503569 | HCID 178503569 | — |
Reaktionsschritte
A solution of 4,6-dihydroxy-2-methylthiopyrimidine (42 g, 0.257 mol) in trifluoroacetic acid (91 ml, 1.186 mol) was stirred at 23° C. and warmed until all solid had gone into solution. The reaction was stirred for five hours at 23° C. Next, fuming HNO3 (15 ml, 350 mmol) was added portion wise to the reaction mixture over 25 minutes at 0° C. The reaction was stirred for twenty hours at 23° C., and treated with H2O (at 23° C.) at 80% conversion (according LC-MS). The solid precipitate was captured via filteration giving 4,6-dihydroxy-2-methylthio-5-nitropyrimidine as a tan-colored solid. The crude solid was azeotroped with toluene to give 35 g of pale tan powdery solid. 1H-NMR: 300 MHz, (CD3OD, 300 MHz) d (ppm) 2.63 (s, 3H). LCMS-ESI+: calc'd for C5H4N3O4S: 202.0 (M−H−); Found: 202.0 (M−H−).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08367670B2 |
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| Quelldatensatz | uspto-grants-2013_02 |
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| ORD ID | ord-b023a427afb4407a8615ff14abac8306 |
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| Quellennotiz | uspto-grants-2013_02 |
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