HuagongsheHuagongshe Chemistry Print Report · For research reference only
Formaldehyde → HCID 66936524, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Formaldehyde | HCID 712 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 66936270 | HCID 66936270 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 66936524 | HCID 66936524 | 91.2% |
Reaction Steps
To a solution of (2R,5R)-5-ethyl-2-methyl-1-(phenylmethyl)piperazine (prepared according to procedures in J. Med. Chem. 2006, 49, 716-726, utilizing Boc-D-2-aminobutyric acid in place of N-Boc-L-alanine) (902 mg, 4.13 mmol) in dichloromethane (25 mL) at 0° C. was added formaldehyde (0.435 mL, 37% water solution, 5.78 mmol) followed by sodium triacetoxyborohydride (1050 mg, 4.96 mmol). The reaction mixture was allowed to warm to room temperature and stirred for 2 h before being diluted with dichloromethane and washed with 1N NaOH solution. The organics were washed with brine, dried (MgSO4) and evaporated to yield (2R,5R)-2-ethyl-1,5-dimethyl-4-(phenylmethyl)piperazine (875 mg, 91%). LCMS: (M+H)+: 233.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07893056B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-22d6aac2f98a4b2590cff261b9b61000 |
| Source note | uspto-grants-2011_02 |