HuagongsheHuagongshe Chemistry Print Report · For research reference only
Morpholine → 3-nitro-4-valeramidobenzoic Acid Morpholide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 3-nitro-4-(pentanoylamino)benzoic Acid | HCID 11777658 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-nitro-4-valeramidobenzoic Acid Morpholide | HCID 53888756 | — |
Reaction Steps
In tetrahydrofuran (800 ml), 3-nitro-4-valeramidobenzoic acid ([1]-(11)-1) (20.0 g) was dissolved. Dicyclohexylcarbodiimide (17.1 g) and 1-hydroxybenzotriazole (11.2 g) were added to the solution, and the mixture was stirred at room temperature for 15 minutes. Morpholine (7.27 g) was further added to the solution. The mixture was stirred for 16 hours. After the insolubles were removed from the reaction solution, the solution was concentrated and dried. The crude product was dissolved in chloroform, and the insolubles were removed, and the solution was purified by silica gel column chromatography (Kieselgel 60=400 g, chloroform/methanol=30/1) to obtain the compound ([1]-(12)-1) (22.95 g) as yellow needle crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05731310 |
| Source dataset | uspto-grants-1998_03 |
| ORD ID | ord-28db859784404afd8675d326cead07a5 |
| Source note | uspto-grants-1998_03 |