HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 58031793, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | HCID 22687730 | HCID 22687730 | — |
| Reactant | HCID 66628645 | HCID 66628645 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58031793 | HCID 58031793 | — |
Reaction Steps
To a solution of 150 mg (0.67 mmol) of ethyl 3-(4-aminophenyl)-3-methoxypropionate, 116 mg (1.01 mmol) of N-ethylmorpholine, 123 mg (0.81 mmol) of HOBt hydrate and 125 mg (0.81 mmol) of EDAC in 2 ml of DMF was added a solution of 212 mg (0.74 mmol) of 2-(2-bromo-4-isopropylphenoxy)propionic acid in 2 ml of DMF. After 22 h at room temperature, the reaction mixture was diluted with sodium chloride solution and extracted with ethyl acetate. The organic phase was dried over MgSO4, filtered and concentrated under reduced pressure. This gave 331 mg of ethyl 3-{4-[2-(2-bromo-4-isopropylphenoxy)propionylamino]phenyl}-3-methoxypropionate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648038B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-e560ead1b2ec4630be5c60b5bcd48823 |
| Source note | uspto-grants-2014_02 |