HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 71657549, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | P,P-Diphenylphosphinic azide | HCID 199401 | — |
| Reactant | 6-Fluoro-1-(piperidin-4-yl)indoline | HCID 22038384 | — |
| Reactant | 4-Oxo-4,5,6,7-tetrahydropyrazolo[1,5-a] pyrazine-2-carboxylic acid | HCID 55264578 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71657549 | HCID 71657549 | — |
Reaction Steps
To a suspension of 4,5,6,7-tetrahydro-4-oxo-pyrazolo[1,5-a]pyrazine-2-carboxylic acid (181 mg, 1.0 mmol) in THF (15 mL) was added diphenylphosphoryl azide (0.25 mL, 1.0 mmol) and Et3N (0.28 mL. 2.0 mmol). The resulting mixture was heated to reflux for 6 h and cooled to room temperature. Then 6-fluoro-1-(piperidin-4-yl)indoline (88 mg, 0.4 mmol) and Et3N (0.14 mL, 1.0 mmol) were added sequentially. The resulting mixture was stirred at room temperature for 24 h and concentrated. The resulting residue was purified by chromatography using EtOAc, then 2-5% MeOH/EtOAc as the eluent to yield 4-(6-fluoroindolin-1-yl)-N-(4-oxo-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrazin-2-yl)piperidine-1-carboxamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09238658B2 |
| Source dataset | uspto-grants-2016_01 |
| ORD ID | ord-ca856f801a4e40709bd111546ae06473 |
| Source note | uspto-grants-2016_01 |