Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Methanol | HCID 887 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178442549 | HCID 178442549 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 19902507 | HCID 19902507 | — |
Reaction Steps
272 g of 6-cyano-2-(1-ethylpentyl)-7-hydroxy-5-methyl[1,2,4]triazolo[2,3-a]pyridine were introduced into 250 g of phosphorus oxytrichloride and stirred at 105° C. for 4 hours. Then 250 g of methanol were added dropwise, the mixture was briefly boiled and 250 ml of water were run in. The solution was cooled and, at 10° to 20° C., the pH was adjusted to 7.5 with aqueous ammonia, when the target product precipitated. It was filtered off with suction, washed with water and dried at 50° C. under reduced pressure. 264 g of the compound of the formula ##STR11## were obtained. A sample recrystallized from ethanol/cyclohexane has a melting point of 95° to 96° C. and the following analysis:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05101028 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-ba861e0bc57a45cab02bc64ba82b5acb |
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| Source note | uspto-grants-1992_03 |
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