Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Peracetic Acid | HCID 6585 | — |
| Reactant | 2,4-Diamino-6-chloropyrimidine | HCID 67432 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 178507684 | HCID 178507684 | — |
Reaction Steps
144.5 g. of 2,4-diamino-6-chloropyrimidine are suspended in 2000 ml. of ethanol. While stirring, the suspension is warmed to 35° C. (about 15 minutes), the greater part of the substance passing into solution. The mixture is then cooled to 6°-8° C. and, at this temperature, there are added dropwise within the course of 40 minutes 175 ml. of 40% peracetic acid in glacial acetic acid. After completion of the addition, the mixture is stirred at 6°-8° C. for a further 30 minutes. The mixture is then left to warm up to room temperature and stirred at this temperature for 3 hours. 2000 Ml. of petroleum ether are then added, the mixture is left to stir for 1 hour and then left to stand overnight. The separated precipitate is filtered off, back-washed with 200 ml. of petroleum ether and dried under reduced pressure, there being obtained 2,4-diamino-6-chloropyrimidine-3-oxide. Recrystallization yields analytically-pure product having a melting point of 193° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04220772 |
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| Source dataset | uspto-grants-1980_09 |
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| ORD ID | ord-d34113bcc99e43e198cce663f85dd86d |
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| Source note | uspto-grants-1980_09 |
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