HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → 2-{[(4-Fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-5-(4-morpholinylcarbonyl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 3-Methyl-1,2-oxazol-4-amine hydrochloride | HCID 13804285 | — |
| Reactant | 2-{[(4-Fluorophenyl)methyl]oxy}-5-(4-morpholinylcarbonyl)benzoic acid | HCID 67107235 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-{[(4-Fluorophenyl)methyl]oxy}-N-(3-methyl-4-isoxazolyl)-5-(4-morpholinylcarbonyl)benzamide | HCID 68109048 | — |
Reaction Steps
3-Methyl-4-isoxazolamine hydrochloride (44.9 mg, 0.33 mmol), 1-hydroxy-7-azabenzotriazole (41.7 mg, 0.31 mmol), diisopropylethylamine (0.10 ml, 0.56 mmol) and EDC (80 mg, 0.42 mmol) were added to a solution of 2-{[(4-fluorophenyl)methyl]oxy}-5-(4-morpholinylcarbonyl)benzoic acid (100 mg, 0.28 mmol) in N,N-dimethylformamide (5 ml). The solution was stirred for 18 hours before the solvent was removed in vacuo. The residue purified by column chromatography (silica gel; 10% 7M NH3 in methanol/dichloromethane). Trituration with methanol yielded the title compound as a white solid. 21 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08778939B2 |
| Source dataset | uspto-grants-2014_07 |
| ORD ID | ord-6621abea39634728aea1a97d3815bbf6 |
| Source note | uspto-grants-2014_07 |