Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Cyclopropylboronic acid | HCID 2760897 | — |
| Reactant | 2-(phenoxymethyl)-6,7-dihydropyrazolo[1,5-a]pyrazin-4(5H)-one | HCID 57411799 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Catalyst | Cupric acetate monohydrate | HCID 165397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 67973582 | HCID 67973582 | 16.4% |
Reaction Steps
Copper(II) acetate monohydrate (83 mg, 041 mmol) was added to a mixture of 2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one (0.1 g, 0.41 mmol), cyclopropylboronic acid (35 mg, 0.41 mmol) and DMAP (75 mg, 0.617 mmol) in toluene (1 mL). The mixture was stirred at 95° C. for 16 hours. The mixture was stirred at 95° C. for 24 hours more. The reaction was allowed to room temperature and was poured into a 1N solution of HCl and extracted with AcOEt. The organic layer was separated, dried (Na2SO4), filtered and concentrated in vacuo. The crude product was purified by flash column chromatography (silica; AcOEt in DCM 0/100 to 50/50). The desired fractions were collected and the solvents evaporated in vacuo. The desired product was triturated with diethyl ether to yield 5-cyclopropyl-2-phenoxymethyl-6,7-dihydro-5H-pyrazolo[1,5-a]pyrazin-4-one (19 mg, 16% yield) as a white solid. 1H NMR (500 MHz, CDCl3) δ ppm 0.68-0.79 (m, 2H), 0.89-1.00 (m, 2H), 2.74-2.82 (m, 1H), 3.74-3.82 (m, 2H), 4.30-4.37 (m, 2H), 5.08 (s, 2H), 6.93 (s, 1H), 6.94-6.97 (m, 1H), 6.98-7.02 (m, 2H), 7.26-7.31 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08592422B2 |
|---|
| Source dataset | uspto-grants-2013_11 |
|---|
| ORD ID | ord-5ad8d904dbea430a81c28dc32f3aa904 |
|---|
| Source note | uspto-grants-2013_11 |
|---|