Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methane | HCID 297 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Sodium Nitrate | HCID 24268 | — |
| Reactant | Phosphinic Acid | HCID 4124402 | — |
| Reactant | HCID 178478804 | HCID 178478804 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178512685 | HCID 178512685 | 5% |
Reaction Steps
A mixture of 42 ml of concentrated sulfuric acid and 21 ml of water was cooled to -10° and 1.56 g (22.7 mmol) of sodium nitrate was added. Afrer stirring at -5° for ten minutes, 8.1 ml (78 mmol) of cold 50% hypophosphorous acid was added and stirring was continued for another 10 minutes at -5°. A solution of 2.5 g (8.4 mmol) of 2-guanidino-4-(2-amino- 4-imidazoyl)thiazole dihydrochloride in 100 ml of water was added dropwise over 0.5 hour. The reaction was stirred at 50° for 2 hours, then at room temperature for 16 hours. The reaction mixture was diluted with 500 ml of water, made basic with solid sodium carbonate and extracted three times with 150 ml portions of ethyl acetate. The combined ethyl acetate extracts were dried over sodium sulfate, filtered, and evaporated leaving a solid. This solid was taken up into boiling methanol, decolorized with charcoal, and concentrated to a small volume. The resulting solid was collected and dried, thereby affording 90 mg (5%) of 2-guanidino-4-(4-imidazoyl)thiazole identical to the material of Example 31 by thin layer chromatography and high resolution mass spectrometry.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590299 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-a8f3e8f973ed4595bfb1375bb888cc75 |
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| Source note | uspto-grants-1986_05 |
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