HuagongsheHuagongshe Chemistry Print Report · For research reference only
Furfural → 3-(4-Fur-2-ylmethylamino-1-oxoisoindolin-2-yl)-5-hydroxypiperidine-2,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Furfural | HCID 7362 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-(4-Amino-1-oxoisoindolin-2-yl)-5-hydroxypiperidine-2,6-dione | HCID 9965376 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 3-(4-Fur-2-ylmethylamino-1-oxoisoindolin-2-yl)-5-hydroxypiperidine-2,6-dione | HCID 22241178 | — |
Reaction Steps
A solution of 3-(4-amino-1-oxoisoindolin-2-yl)-5-hydroxypiperidine-2,6-dione (0.82 g, 3.0 mmol) and 2-furaldehyde (0.34 g, 3.5 mmol) in acetic acid (10 mL) is heated at reflux for 4 hours. To the mixture is added sodium borohydride (130 mg, 3.5 mmol) at room temperature and kept for 18 hours. The mixture is worked up to give 3-(4-fur-2-ylmethylamino-1-oxoisoindolin-2-yl)-5-hydroxypiperidine-2,6-dione which is further purified by column chromatography.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07005438B2 |
| Source dataset | uspto-grants-2006_02 |
| ORD ID | ord-9d832ab939a84708930c2090ed664362 |
| Source note | uspto-grants-2006_02 |