HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromo-N-phenylacetamide → Ethyl 3-{(5-oxo-1-(3-{((n-phenylcarbamoyl)methyl)amino}phenyl)pyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromo-N-phenylacetamide | HCID 94818 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Ethyl 3-{(1-(3-aminophenyl)-5-oxopyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoate | HCID 10200775 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 3-{(5-oxo-1-(3-{((n-phenylcarbamoyl)methyl)amino}phenyl)pyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoate | HCID 12135100 | — |
Reaction Steps
To a suspension of ethyl 3-{(1-(3-aminophenyl)-5-oxopyrrolidin-3-yl)carbonylamino}-3-(3-pyridyl)propanoate (100 mg, 0.25 mmol, 1.1 eq), NaHCO3 (20 mg, 0.23 mmol, 1.0 eq), and CH2Cl2 (4 mL), was added 2-bromo-N-phenyl acetamide (50 mg, 0.23 mmol, 1.0 eq) in 2 mL CH2Cl2 dropwise. The reaction mixture was heated up to reflux for 5 hours, then cooled to room temperature.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06849639B2 |
| Source dataset | uspto-grants-2005_02 |
| ORD ID | ord-3bd8776ed88845958bb2ae80031c161d |
| Source note | uspto-grants-2005_02 |