Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Nitric Acid | HCID 944 | — |
| Reactant | 2-(Propylthio)pyrimidine-4,6-diol | HCID 178460810 | — |
| Product | HCID 178460811 | HCID 178460811 | — |
Reaction Steps
To a clean and dry reaction assembly containing acetic acid (1000 ml) was added fuming nitric acid (340 ml) over a period of 15 to 20 minutes, while maintaining the temperature between 25-30° C. 2-Propylthio-pyrimidine-4,6-diol (400 g) was added to the mixture over a period of 60 minutes at 25-30° C., followed by rinsing of flask with acetic acid (100 ml). The resulting mass was stirred for 1 hour at 25-30° C. After completion of the reaction, water (2400 ml) was added to the mass for 20 minutes at 25-30° C. The resulting slurry was stirred for 1 hour at 25-30° C. The product was isolated by filtration and washed successively with water (4×800 ml). The wet product was dried under reduced pressure at 50-55° C. to produce the 5-nitro-2-propylthiopyrimidine-4,6-diol as a off-white to yellow powder (375 g, HPLC purity: 99.06% by area).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08859769B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-09c017fabb154758b12e63ce322da674 |
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| Source note | uspto-grants-2014_10 |
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