HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 2-(1-Benzyloxy-carbonyl-piperidin-4-yl)-5-chloro-7-morpholin-4-yl-pyrazolo[1,5-a]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 2-(1-Benzyloxy-carbonyl-piperidin-4-yl)-5,7-dichloro-pyrazolo[1,5-a]-pyrimidine | HCID 86659732 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(1-Benzyloxy-carbonyl-piperidin-4-yl)-5-chloro-7-morpholin-4-yl-pyrazolo[1,5-a]pyrimidine | HCID 86659731 | 88% |
Reaction Steps
There was dissolved, in 1,4-dioxane (5 mL), 2-(1-benzyloxy-carbonyl-piperidin-4-yl)-5,7-dichloro-pyrazolo[1,5-a]-pyrimidine (192 mg, 0.474 mM), then morpholine (82.7 μL, 0.948 mM) was added to the solution and the mixture was stirred at room temperature for one hour. The solvent was distilled off from this reaction mixture, the residue thus obtained was diluted with water and then the mixture was extracted with ethyl acetate. The resulting extracts were combined, dried over anhydrous sodium sulfate, the solvent was distilled off and the resulting solid was washed with diethyl ether to thus give the title compound (191 mg, yield: 88%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08314098B2 |
| Source dataset | uspto-grants-2012_11 |
| ORD ID | ord-a295b00352dd477e87bbc62737850594 |
| Source note | uspto-grants-2012_11 |