HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-3-Cyclobutyl-2-{(S)-3-(3-fluoro-phenyl)-4-[4-(3-phenyl-propyl)-piperidin-1-ylmethyl]-pyrrolidin-1-yl}-propionic acid → 2-(r)(3-(s)-((4-(3-(2,6-Difluorophenyl)propyl)piperidin-1-yl)methyl)-4-(s)-(3-fluorophenyl)pyrrolidin-1-yl)-3-cyclobutylpropanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-3-Cyclobutyl-2-{(S)-3-(3-fluoro-phenyl)-4-[4-(3-phenyl-propyl)-piperidin-1-ylmethyl]-pyrrolidin-1-yl}-propionic acid | HCID 20672386 | — |
| Reactant | 4-(3-(2,6-Difluorophenyl)propyl)piperidine | HCID 21180778 | — |
| Product | 2-(r)(3-(s)-((4-(3-(2,6-Difluorophenyl)propyl)piperidin-1-yl)methyl)-4-(s)-(3-fluorophenyl)pyrrolidin-1-yl)-3-cyclobutylpropanoic acid | HCID 20672343 | — |
Reaction Steps
The title compound was prepared from 2-(R)-(3-(R)-formyl-4-(S)-(3-fluorophenyl)pyrrolidin-1-yl)-3-(cyclobutyl)propanoic acid, benzyl ester (from EXAMPLE 26, Step A) and 4-(3-(2,6-difluorophenyl)propyl) piperidine.HCl (from EXAMPLE 114, Step A) using procedures analogous to those described in EXAMPLE 1, Steps J and K to provide the title compound: ESI-MS 543 (M+H); HPLC (YMC ODS-A 4.6×50 mm column, gradient elution using 10:90 v/v CH3CN/H2O+0.1% TFA to 100% CH3CN +0.1% TFA over 2.0 min, hold 1 min, 5.0 mL/min, 220 nm): Retention Time: 1.34 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265434B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-4673b554d2f44110a1da8c9bff13cdf8 |
| Source note | uspto-grants-2001_07 |