HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → 2-Amino-5-chloro-8-methoxy[1,2,4]triazolo[1,5-a]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Hydroxyamine hydrochloride | HCID 443297 | — |
| Reactant | N-(6-Chloro-3-methoxy-2-pyridinyl)-N'-carboethoxythiourea | HCID 21464341 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Amino-5-chloro-8-methoxy[1,2,4]triazolo[1,5-a]pyridine | HCID 18366195 | 58.6% |
Reaction Steps
Hydroxylamine hydrochloride (9.6 g, 138 mmol) and diisopropylethylamine (14.4 mL, 10.7 g, 83 mmol) were mixed with ethanol (300 mL) for a few minutes and then N-(6-chloro-3-methoxy-2-pyridinyl)-N'-carboethoxythiourea (7.6 g, 27.5 mmol) was added with stirring. The resulting mixture was stirred at room temperature for 20 min and then heated to reflux for 3 hours. The volatile components were removed by evaporation and the residue obtained was mixed with water. The resulting slurry was filtered and the solids collected were washed with ether, a small amount of methanol, and finally hexane and were then dried. The title compound (3.2 g) was obtained as a tan powder melting at 207°-208° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05700940 |
| Source dataset | uspto-grants-1997_12 |
| ORD ID | ord-2e93278c6de64f08ad22b94276dcdead |
| Source note | uspto-grants-1997_12 |