HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → N-[2-(3,4-Dimethoxyphenyl)-ethyl]-2-(4-fluorophenyl)-2-formylaminoacetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | 2,3-Dimethoxyphenethylamine | HCID 137858 | — |
| Reactant | O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate | HCID 2733207 | — |
| Reactant | N-formyl-4-fluorophenylglycine | HCID 86761449 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-[2-(3,4-Dimethoxyphenyl)-ethyl]-2-(4-fluorophenyl)-2-formylaminoacetamide | HCID 86761448 | — |
Reaction Steps
To a mixture of N-formyl-4-fluorophenylglycine (900 mg) and 2,3-dimethoxyphenethylamine (1 ml) in DMF (5 ml) was added N-ethylmorpholine (0.75 ml) and TBTU (1.6 g). After stirring for 4 h, the reaction was quenched by addition of water (30 ml). The product was extracted with ethylacetate. The organic layer was washed with water, dried (MgSO4), filtered and concentrated in vacuo. The residue was triturated with methyl-tert.butylether and recrystallized from toluene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071587B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-e1a2af46a098420786f22507da9aabc3 |
| Source note | uspto-grants-2011_12 |