HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 59321452, compound → Tert-butyl 4-(aminomethyl)-4-(2,3-dichlorophenyl)piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 59321452 | HCID 59321452 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ammonia | HCID 222 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | Tert-butyl 4-(aminomethyl)-4-(2,3-dichlorophenyl)piperidine-1-carboxylate | HCID 59321370 | — |
Reaction Steps
Tert-butyl 4-cyano-4-(2,3-dichlorophenyl)piperidine-1-carboxylate (2.30 g, 6.47 mmol) was dissolved in 75 ml of a 7M solution of NH3 in MeOH. Raney Nickel (˜2 g aq. suspension) was added and the mixture shaken on a PARR apparatus under 60 psi of hydrogen for 4 days. The catalyst was removed by filtration through a layer of Celite and the crude reaction mixture concentrated. The crude product (1.90 g yellow oil) was used in the next reaction (amide bond formation) “as is”.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08343999B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-c74be3264331470aaac52b37e03979e6 |
| Source note | uspto-grants-2013_01 |