HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Ammonium hydroxide methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Tetrahydro-4H-pyran-4-one | HCID 121599 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 68599587 | HCID 68599587 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11567437 | HCID 11567437 | — |
| Product | Ammonium hydroxide methanol | HCID 21894508 | 1% |
Reaction Steps
To a solution of (1R,3S)-3-isopropyl-3-[(4-phenyl-3,6-dihydropyridin-1(2H)-yl)carbonyl]cyclopentanamine hydrochloride (50 mg, 0.1 mmol), tetrahydro-4H-pyran-4-one (43 mg, 0.43 mmol), and triethylamine (0.070 mL, 0.50 mmol) in methylene chloride (2 mL) was added sodium triacetoxyborohydride (91 mg, 0.43 mmol). After being stirred at room temperature overnight, saturated NaHCO3 was added. The solution was extracted with methylene chloride three times. The combined extracts were dried (MgSO4), filtered, and concentrated. Purification by flash chromatography on silica gel (gradient: 0-15% B over 15 min. Bottle A=1% NH40H/3% MeOH/EtOAc, Bottle B=1% NH4OH/MeOH) afforded the desired compound. MS calculated for C25H36N2O2: (M+H) 397; found 397.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07449467B2 |
| Source dataset | uspto-grants-2008_11 |
| ORD ID | ord-878b34883570433d8c9da80eb5dfc432 |
| Source note | uspto-grants-2008_11 |