Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Formic Acid | HCID 284 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | 5-Nitroso-4,6-pyrimidinediamine | HCID 259752 | — |
| Reactant | Sodium Formate | HCID 2723810 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Formamide | HCID 713 | — |
| Product | Adenine | HCID 190 | 90% |
Reaction Steps
13.9 g (0.1 mol) 4,6-diamino-5-nitrosopyrimidine was suspended in 50 ml formamide, 6.8 g (0.1 mol) sodium formate, 27.0 g (0.5 mol) 85% formic acid and 0.5 g palladium catalyst were added according to example 1 and the mixture was heated for 4 hours to 110° C. The decolorized suspension was subsequently heated for 3 hours to 180° C. and then cooled. In order to improve the processing, 50 ml water was added and the solid was filtered. The filter cake was dissolved in 160 ml 5% sodium hydroxide solution and the insoluble Pd catalyst was separated. The clear filtrate was adjusted with sulphuric acid to a pH value of 8.5 after a 30 minute treatment at 50° C. with 3 g active carbon. In this process a colorless precipitate separated out from adenine which was suction filtered, washed twice with 30 ml water and dried in a vacuum at 80° C. 12.2 g adenine (0.090 mol, 90% of theory) was obtained in this way as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05688947 |
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| Source dataset | uspto-grants-1997_11 |
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| ORD ID | ord-6ca92aea4b424904b29b5ab7c0d216bd |
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| Source note | uspto-grants-1997_11 |
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