Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | Benzenamine, 4-(4-morpholinyl)- | HCID 75655 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2,4-Dibenzyloxy-5-isopropyl-benzoic acid | HCID 59167879 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59829891 | HCID 59829891 | 87% |
Reaction Steps
A dichloromethane (30 mL) solution of 2,4-bis-benzyloxy-5-isopropylbenzoic acid (F370-IM1, 2 g, 5.31 mmol) was mixed with dimethylformamide (0.053 mL, 0.05 mmol) and oxalylchloride (0.61 mL, 6.38 mmol) under ice cold conditions and the mixture was stirred at room temperature overnight. The reaction mixture was concentrated under reduced pressure, and the residue thus obtained was dissolved in tetrahydrofuran (30 mL) and pyridine (10 mL). To the solution was added 4-(4-morpholino)aniline (1.04 g, 5.84 mmol) under ice cold conditions. The reaction was carried out at room temperature for 1 hour. Dichloromethane (50 mL) and 5% aqueous sodium hydrogencarbonate (20 mL) were added to the reaction mixture. The aqueous layer was separated and extracted with dichloromethane, the combined organic layers thus obtained were washed with saturated aqueous sodium chloride solution (30 mL) and dried over anhydrous sodium sulfate. Sodium sulfate was removed by filtration, and the solvent was distilled off under reduced pressure. To the residue were added ethyl acetate (5 mL), toluene (5 mL) and hexane (20 mL), and the resulting suspension was stirred at room temperature for 1 hour. The precipitated solid was collected by filtration to obtain the title compound (F370-IM2: white crystals, 2.47 g, 87%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08399464B2 |
|---|
| Source dataset | uspto-grants-2013_03 |
|---|
| ORD ID | ord-e5e141f929bc46d8afa2f261dc73563c |
|---|
| Source note | uspto-grants-2013_03 |
|---|