HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → N-(3,4-Dimethoxy-phenyl)-N'-methyl-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Methylamine | HCID 6329 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | N-(3,4-Dimethoxy-phenyl)-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acid | HCID 57591457 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(3,4-Dimethoxy-phenyl)-N'-methyl-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamide | HCID 25014479 | 16.3% |
Reaction Steps
A mixture of 16.2 mg (0.033 mmol) N-(3,4-Dimethoxy-phenyl)-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acid, 15.5 mg (0.049 mmol) methylamine (commercially available), 13.8 mg (0.043 mmol) TBTU and 7.8 mg (0.09 mmol) pyridine in 2 mL DMF was shaken for 4 h at room temperature. The mixture was evaporated to dryness, taken up in methanol, formic acid and subjected to purification by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and acetic acid. The combined product fractions were evaporated to dryness to yield 2.7 mg (16%) of the title compound. MS(m/e): 501.3 (MH+), MH+ found: 501.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501541B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-4b9d3f93ebc54ec0bf7376c8f134501f |
| Source note | uspto-grants-2009_03 |