HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 354172Generated: October 31, 2026
Potassium Carbonate → 5-{2-Butoxy-5-[3-(trifluoromethyl)phenyl]-3-pyridinyl}-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7h-pyrazolo[4,3-d]pyrimidin-7-one
https://huagongshe.com/reaction/354172
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Trifluoromethyl)phenylboronic acid | HCID 2734388 | — |
| Reactant | 5-(2-Butoxy-5-iodo-3-pyridinyl)-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one | HCID 135456031 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 5-{2-Butoxy-5-[3-(trifluoromethyl)phenyl]-3-pyridinyl}-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7h-pyrazolo[4,3-d]pyrimidin-7-one | HCID 135730644 | 70% |
Reaction Steps
5-(2-Butoxy-5-iodo-3-pyridinyl)-3-ethyl-2-(2-methoxyethyl)-2,6-dihydro-7H-pyrazolo[4,3-d]pyrimidin-7-one (Example 1) (140 mg, 0.28 mmol), K2CO3 (78 mg, 0.56 mmol) and 3-trifluoromethylboronic acid (60 mg, 0.34 mmol) were stirred together in aqueous dioxan under a nitrogen atmosphere. The mixture was immersed in a pre-heated oil bath at 120° C. for a few minutes and Pd(PPh3)4 (34 mg, 0.028 mmol) was added. The mixture was heated at reflux for 2 h and then cooled. The cooled mixture was concentrated and partitioned between ethyl acetate and water. This was then filtered through an Arbocel® pad to remove the palladium residues and the organic layer separated, washed with sodium bicarbonate solution then brine, dried (MgSO4) and concentrated. Recrystallisation from ethyl acetate gave the title compound (101 mg, 70%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06756373B1 |
|---|
| Source dataset | uspto-grants-2004_06 |
|---|
| ORD ID | ord-fa7e0f3b7abf4ea8897a81890f16500f |
|---|
| Source note | uspto-grants-2004_06 |
|---|