HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(6-Ethoxy-5-formyl-3-pyridylsulfonyl)-4-ethylpiperazine → 4-{6-ethoxy-5-[3-ethyl-4,5,6,7-tetrahydro-7-oxo-2-(2-pyridylmethyl)-2H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-pyridinylsulfonyl}-1-ethylpiperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(6-Ethoxy-5-formyl-3-pyridylsulfonyl)-4-ethylpiperazine | HCID 22052236 | — |
| Reactant | 4-amino-5-ethyl-1-(2-pyridylmethyl)-1H-pyrazole-3-carboxamide | HCID 22052237 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-{6-ethoxy-5-[3-ethyl-4,5,6,7-tetrahydro-7-oxo-2-(2-pyridylmethyl)-2H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-pyridinylsulfonyl}-1-ethylpiperazine | HCID 22052233 | 52% |
Reaction Steps
A solution of 1-(6-ethoxy-5-formyl-3-pyridylsulfonyl)-4-ethylpiperazine(1.1 g, 4.9 mmol, from step (a) above) and 4-amino-5-ethyl-1-(2-pyridylmethyl)-1H-pyrazole-3-carboxamide (1.2 g, 4.9 mmol) in toluene (10 mL) was heated to reflux for 4 hours and the solution was concentrated under vacuum. The resulting product was recrystallised from ethyl acetate to give a pale brown solid (1.4 g, 52%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07067660B2 |
| Source dataset | uspto-grants-2006_06 |
| ORD ID | ord-806039f3b87c4aab968ec134fb833c16 |
| Source note | uspto-grants-2006_06 |