HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methylamine → 2-(3-Ethyl-ureido)-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid methylamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 2-(3-Ethyl-ureido)-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid methyl ester | HCID 44571954 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-(3-Ethyl-ureido)-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid methylamide | HCID 44572001 | — |
Reaction Steps
2-(3-Ethyl-ureido)-7-pyridin-3-yl-[1,2,4]triazolo[1,5-a]pyridine-5-carboxylic acid methyl ester, prepared as in Example 6, (46 mg, 0.14 mmol) was suspended/dissolved in 33% methylamine in EtOH (15 mL), then stirred overnight at room temperature. After this time the reaction mixture was concentrated to a volume of ca 5 mL, then diluted with Et2O (5 mL). The resulting precipitate was isolated by filtration and washed well with Et2O to give the final product mp. >300° C. LCMS (APCI+) 340.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07524860B2 |
| Source dataset | uspto-grants-2009_04 |
| ORD ID | ord-443389a7ee3040359fd7d9f20ad731df |
| Source note | uspto-grants-2009_04 |