Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-Chlorohypoxanthine hydrochloride monohydrate | HCID 135588821 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Chlorohypoxanthine | HCID 135421792 | — |
Reaction Steps
180 g (0.80 mol) of 2-chlorohypoxanthine-hydrochloride-monohydrate are suspended in 3.6 liters of water and the pH is adjusted to 6.5 by the dropwise addition of concentrated sodium hydroxide solution. After heating to 60° C. the solution is treated with 18 g of decolorising charcoal and filtered. The filtrate is added dropwise to 300 ml of water, whilst a pH of 3.0 +/- 0.5 is maintained in the aqueous solution using 1N hydrochloric acid. The resulting suspension is cooled to 5°-10° C., suction filtered and the precipitate is washed with 0.5 liters of water at a temperature of +5° C. and with 300 ml of isopropanol. After drying at 50° C., 117 g (85.8% of theory) of the title compound are obtained in the form of a colourless crystal powder. By purifying via the sodium salt and re-liberation of the base, analytically pure material is obtained which is identical to the substance prepared from 2,6-dichloropurine according to J. A. Montgomery and L. B. Holum [J. Am. Chem. Soc. 79 (957) 2185].
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05264573 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-e5485da746d446939fcd07e9e942a705 |
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| Source note | uspto-grants-1993_11 |
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