HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Carbonate → 3-amino-1-[{4-(2,4-dimethylphenyl)piperazin-1-yl}propanoyl]-6-N-benzyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-Chloro-1-{4-(2,4-dimethylphenyl)piperazin-1-yl}propan-1-one | HCID 67997080 | — |
| Reactant | t-Butyl-3-amino-6-benzyl-4,5,6,7-tetrahydro-7-oxapyrazolo[3,4-c]pyridin-1-carboxylate | HCID 67997531 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-amino-1-[{4-(2,4-dimethylphenyl)piperazin-1-yl}propanoyl]-6-N-benzyl-4,5,6,7-tetrahydro-1H-pyrazolo[3,4-c]pyridin-7-one | HCID 67997005 | 11.6% |
Reaction Steps
Potassium carbonate (68.2 mg, 0.494 mmol) was added to a solution of t-butyl-3-amino-6-benzyl-4,5,6,7-tetrahydro-7-oxapyrazolo[3,4-c]pyridin-1-carboxylate (154 mg, 0.449 mmol) dissolved in anhydrous acetonitrile (1.9 mL) and then stirred at room temperature for 30 minutes. After adding 3-chloro-1-{4-(2,4-dimethylphenyl)piperazin-1-yl}propan-1-one (132.2 mg, 0.471 mmol), reaction was carried out overnight. A target compound (25.4 mg, 0.052 mmol, 11.6%) was yielded as white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08383631B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-53e1d2ac111147d79360de6a2da78ad2 |
| Source note | uspto-grants-2013_02 |