HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → CBz-D-phenylglycine 4-(1-methylpiperidin-4-yl)piperidinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | CBz-D-phenylglycine 4-[l-(Boc)piperidin-4-yl]piperidinamide | HCID 131722771 | — |
| Solvent | Formaldehyde | HCID 712 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | CBz-D-phenylglycine 4-(1-methylpiperidin-4-yl)piperidinamide | HCID 131722772 | 97% |
Reaction Steps
To a solution of CBz-D-phenylglycine-4-[1-(Boc)piperidin-4-yl]piperidinamide (1.1 g, 2.5 mmol) in acetonitrile (40 ml) and aq. formaldehyde (10 ml) was added sodium cyanoborohydride (315 mg, 5 mmol) portionwise over 10 min. The reaction mixture was left to stir for 3 hours and then poured onto water (50 ml), containing conc ammonia solution (5 ml) and left to stir for 15 min. Extraction with ethyl acetate (100 ml), washing with brine and drying gave the title compound as a colourless oil (1.1 g, 97%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06262069B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-03d5a1bf5b2c4f249a7faa778fcaca45 |
| Source note | uspto-grants-2001_07 |