HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 58031814, 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 66628683 | HCID 66628683 | — |
| Reactant | HCID 66628746 | HCID 66628746 | — |
| Solvent | Sodium Chloride | HCID 5234 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58031814 | HCID 58031814 | — |
Reaction Steps
A solution of 150 mg (0.56 mmol) of ethyl 3-(4-aminophenyl)hex-4-ynoate, 193 mg (1.68 mmol) of N-ethylmorpholine, 103 mg (0.67 mmol) of HOBt hydrate and 104 mg (0.67 mmol) of EDAC in 3 ml of DMF was added to a solution of 160 mg (0.62 mmol) of 2-(5-bromo-2-methylphenoxy)propionic acid in 2 ml of DMF. After 3 days 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 ethyl 3-{4-[2-(5-bromo-2-methylphenoxy)propionylamino]phenyl}hex-4-ynoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648038B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-c2e43067d6a64d1d91d3613308822a8c |
| Source note | uspto-grants-2014_02 |