Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | 1-Boc-3,3-dimethylpiperazine | HCID 22710387 | — |
| Catalyst | Acetic Acid | HCID 176 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 59454538 | HCID 59454538 | — |
Reaction Steps
Tert-butyl 3,3-dimethylpiperazine-1-carboxylate (413 mg, 1.65 mmol) was dissolved in DCE (15 mL). TEA (1.148 mL, 8.23 mmol) was added, followed by cyclobutanone (231 mg, 3.29 mmol) and sodium triacetoxyborohydride (524 mg, 2.47 mmol). The reaction mixture was stirred for 5 h and a few drops of acetic acid were added. The reaction mixture was heated at 40° C. for 4 days, cooled to rt, washed with sat NaHCO3, dried over MgSO4, filtered and concentrated under reduced pressure to give a dark yellow oil. The crude title compound was used in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08993577B2 |
|---|
| Source dataset | uspto-grants-2015_03 |
|---|
| ORD ID | ord-0b8d3ebda5a74d39b2ada77e11564112 |
|---|
| Source note | uspto-grants-2015_03 |
|---|