HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-(4-Hydroxyphenyl)propionic acid → N-(2,4-difluorobenzyl)-3-(4-hydroxyphenyl)-N-propylpropanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-(4-Hydroxyphenyl)propionic acid | HCID 10394 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | [(2,4-Difluorophenyl)methyl](propyl)amine | HCID 24690356 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-(2,4-difluorobenzyl)-3-(4-hydroxyphenyl)-N-propylpropanamide | HCID 69120491 | 68.4% |
Reaction Steps
3-(4-Hydroxyphenyl)propionic acid (245 mg, 1.474 mmol) in DMF (5 ml) was cooled in an ice-bath. N-(2,4-Difluorobenzyl)-N-propylamine (300.4 mg, 1.622 mmol) was added and then TBTU (521 mg, 1.622 mmol) followed by DIPEA (400 mg, 3.096 mmol). The mixture was stirred at room temperature overnight. Sodium hydrogencarbonate aqueous solution (sat.) was added. The mixture was extracted with ethyl acetate (×2). The extracts were combined and dried (magnesium sulphate) and evaporated. Chromatography of the residue on a column (ISOLUTE® SI, 5 g/25 ml) using DCM/heptane (50:50), DCM and then MeOH/DCM (1:99, then 2:98) as eluant gave 336 mg the desired product, yield 68%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07355069B2 |
| Source dataset | uspto-grants-2008_04 |
| ORD ID | ord-3ce818fdfd1441a98695c0d1f53b0c77 |
| Source note | uspto-grants-2008_04 |