HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Acetate → 1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Acetate | HCID 517165 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 1-(3-Phenylpropionyl)-4-ketopiperidine | HCID 17817612 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(4-Aminopiperidin-1-yl)-3-phenylpropan-1-one | HCID 16793772 | 47% |
Reaction Steps
To 3.2 g (13.8 mmol) of 135 in 125 mL of anhydrous methanol was added 21.3 g of ammonium acetate and 20 g of 3A molecular sieves. After stirring 30 min, 3.47 g (55.2 mmol) of sodium cyanoborohydride was added portionwise with stirring. After 3 hours, the mixture was gravity filtered, and the methanol evaporated under vacuum. The residue was partitioned between ice/HCl and ether. The acidic aqueous phase was extracted twice more with ether. The aqueous phase was made basic with ice and 50% aqueous NaOH. The mixture was extracted with CH2Cl2, dried, and evaporated under vacuum to give 1.5 g (47%) of the title amine 136. GC/MS indicated 100% purity with a molecular ion of 232.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06521622B1 |
| Source dataset | uspto-grants-2003_02 |
| ORD ID | ord-00b43c1f6c564e99953d86921cd77417 |
| Source note | uspto-grants-2003_02 |