HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-cyclohexylpiperidin-4-amine → (2R)-2-(BOC)amino-N-[4-(cyclohexylamino)piperidine-1-yl]-3-(4-chlorophenyl)propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-cyclohexylpiperidin-4-amine | HCID 4778242 | — |
| Reactant | N-Boc-4-chloro-D-phenylalanine | HCID 7018791 | — |
| Reactant | (3S)-3-{cyclohexyl[(N-BOC)aminoacetyl]amino}pyrrolidine | HCID 67343482 | — |
| Product | (2R)-2-(BOC)amino-N-[4-(cyclohexylamino)piperidine-1-yl]-3-(4-chlorophenyl)propionamide | HCID 67345059 | — |
Reaction Steps
The title compound was prepared following the procedure described in Intermediate 129 using (2R)-2-(BOC)amino-3-(4-chlorophenyl)propionic acid and 4-[(cyclohexyl)amino]piperidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07989634B2 |
| Source dataset | uspto-grants-2011_08 |
| ORD ID | ord-9f15c565369e48e2a12b52c72d969ff7 |
| Source note | uspto-grants-2011_08 |