HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N1-[1-(4-biphenylyl)-2-(1-pyrrolidinyl)ethyl]-N2-(3 4-dichlorophenyl)-N1,2-dimethylalaninamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Reactant | 1-([1,1'-Biphenyl]-4-yl)-N-methyl-2-(pyrrolidin-1-yl)ethan-1-amine | HCID 2756716 | — |
| Reactant | Lithium | HCID 3028194 | — |
| Reactant | HCID 17605983 | HCID 17605983 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N1-[1-(4-biphenylyl)-2-(1-pyrrolidinyl)ethyl]-N2-(3 4-dichlorophenyl)-N1,2-dimethylalaninamide | HCID 59809575 | — |
Reaction Steps
N-(3,4-dichlorophenyl)-2-methylalanine, lithium salt (100 mg, 0.4 mmol), [1-(4-biphenylyl)-2-(1-pyrrolidinyl)ethyl]methylamine (124 mg, 0.44 mmol), triethylamine (246 uL, 1.77 mmol), and (1 H-1,2,3-benzotriazol-1-yloxy)[tris(dimethylamino)]phosphonium hexafluorophosphate (BOP Reagent, 215 mg, 0.486 mmol) were added in that order to a 4 mL screw capped vial that contained 2 mL of anhydrous DMF. The reaction mixture was stirred for 20 hours at room temperature, then filtered through a 0.45 um PTFE Acrodisk, and purified by reverse-phase HPLC (Xterra Prep RP C-18, 30×150 mm, 50 mL/min, A: acetonitrile B: water, pH 10 w/NH4OH, A: 20 to 99% over 9 min, UV detection at 214 nm) to give the title compound as a white solid. MS (ES) m/e 510 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07432258B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-60be9f7116f742548b4dd8470cbdedff |
| Source note | uspto-grants-2008_10 |