HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(3,4-Dimethoxy-phenyl)-2-methyl-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 57591499 | HCID 57591499 | — |
| Reactant | 2-Chlorocarbonyl-2-phenyl-propionic acid ethyl ester | HCID 86623641 | — |
| Product | N-(3,4-Dimethoxy-phenyl)-2-methyl-2-phenyl-N-[2-(4-trifluoromethyl-phenyl)-ethyl]-malonamic acid ethyl ester | HCID 67084343 | 45% |
Reaction Steps
A mixture of 97.5 mg (0.3 mmol) (3,4-dimethoxy-phenyl)-[2-(4-trifluoromethyl-phenyl)-ethyl]-amine (intermediate 1), 101 mg (0.45 mmol) 2-chlorocarbonyl-2-phenyl-propionic acid ethyl ester (Journal of Organic Chemistry (1959), 24 109-10) and 121 mg (1.2 mmol) triethylamine 15 mL DCM was stirred for 16 h at room temperature. The mixture was evaporated and purified by preparative HPLC on reversed phase eluting with a gradient formed from acetonitrile, water and formic acid, the product containing fractions were evaporated to yield 71.5 mg (45%) of the title compound. MS(m/e): 530.2 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501541B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-a175a90011cb4823bf69fdab4ee0fdf5 |
| Source note | uspto-grants-2009_03 |