HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → (S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Glutaraldehyde | HCID 3485 | — |
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Tetrahydrofurane dichloromethane | HCID 21919333 | — |
| Reactant | phthalimido-(S)-phenyalanine amide | HCID 53840537 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (S)-N-[2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-oxo-3-phenylpropyl]-1,4-dihydro-pyridine | HCID 15380836 | — |
Reaction Steps
Combine phthalimido-(S)-phenyalanine amide (3.0 g, 10 mmol) and a solution of glutaric dialdehyde (2.0 g, 50% by weight in water) in dichloromethane (200 mL). Heat to reflux with azeotropic removal of water from the refluxate. Add p-toluenesulfonic acid (60 mg). Continue heating at reflux. Pass the refluxate through oven dried 4 Å molecular sieves. After 4 days, cool the reaction mixture to ambient temperature. Extract with 5% sodium bicarbonate solution. Extract the 5% sodium bicarbonate solution with dichloromethane. Combine the organic layers and dry over Na2SO4, filter, and evaporate in vacuo to give a residue. Chromatograph the residue on silica gel eluting with 5% tetrahydrofuran/dichloromethane to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05859252 |
| Source dataset | uspto-grants-1999_01 |
| ORD ID | ord-84c3eb894d9f40a3a9fc5b2f015a416a |
| Source note | uspto-grants-1999_01 |