HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 178450148, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 178450149 | HCID 178450149 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178450148 | HCID 178450148 | — |
Reaction Steps
Piperidine in methanol (20%; 2 mL) was added to {1-(4-tert-butoxy-benzyl)-2-oxo-2-[3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-ethyl}-carbamic acid 9H-fluoren-9-ylmethyl ester (0.20 g, 0.28 mmol) at room temperature. After 30 minutes the reaction was concentrated under reduced pressure, and the residual 200 mg of desired product 2-amino-3-(4-tert-butoxy-phenyl)-1-[3-(4-phenyl-1H-imidazol-2-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-propan-1-one was used as is without further purification (LC/MS; Measured, MW (MH+):495).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07202381B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-c5bf65ca101f4c9e9b9313568e52711f |
| Source note | uspto-grants-2007_04 |