Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Maleimidophenyl isocyanate | HCID 129975 | — |
| Reactant | Rac-6-chloro-3-(3-chloro-benzyl)-3-piperidin-3-yl-1,3-dihydro-indol-2-one | HCID 57803070 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 11999358 | HCID 11999358 | 28.3% |
Reaction Steps
To a solution of rac-6-chloro-3-(3-chloro-benzyl)-3-piperidin-3-yl-1,3-dihydro-indol-2-one (80 mg, 0.21 mmol) (from Example 25a supra) in dichloromethane (3 mL) was added triethylamine (32.4 mg, 0.32 mmol) (Aldrich), followed by the addition of 1-(4-isocyanato-phenyl)-pyrrole-2,5-dione (50 mg, 0.23 mmol) (Fluka). The mixture was stirred at room temperature for 0.5 hour. The mixture was partitioned between dichlormethane and water. The aqueous layer was extracted with dichlormethane. The combined organic layer was washed with water, brine, dried over MgSO4 and concentrated. The residue was purified by chromatography to give rac-3-[6-chloro-3-(3-chloro-benzyl)-2-oxo-2,3-dihydro-1H-indol-3-yl]-piperidine-1-carboxylic acid [4-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-phenyl)-amide as a white solid (Yield 35 mg, 28%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07576082B2 |
|---|
| Source dataset | uspto-grants-2009_08 |
|---|
| ORD ID | ord-30c7b99606864d04b71b637d74bde96a |
|---|
| Source note | uspto-grants-2009_08 |
|---|