HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Furoic acid → 1-[(2-Furanyl)carbonyl]-4-(6-methoxy-indan-1-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Furoic acid | HCID 10268 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | (6-Methoxy-indan-1-yl)piperazine | HCID 22038119 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Chlorine | HCID 24526 | — |
| Product | 1-[(2-Furanyl)carbonyl]-4-(6-methoxy-indan-1-yl)piperazine | HCID 22375397 | — |
Reaction Steps
A solution of (-)-(6-methoxy-indan-1-yl)piperazine (28 mg, 0.12 mmol), 3-furoic acid (58 mg, 0.52 mmol), and 1-hydroxybenzotriazole (17 mg, 0.126 mmole), and 1,3-diisopropylcarbodiimide (16 mg, 0.126 mmol) in CH2 Cl2 (2 ml) and DMF (2 ml), was shaken for for 5 min and allowed to stand for 18 hr. The reaction mixture was filtered through an SCX Bondesil® (Varian # 1221-3039, 1 g) column. The column was washed with methanol (20 ml) and 0.1N NH4OH in methanol (2 ml). The product was then eluted from the column using 1N NH4OH in methanol (5 ml). This last fraction was concentrated in vacuo to give the product (36.8 mg, 94%, ES-MS: 327 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05780470 |
| Source dataset | uspto-grants-1998_07 |
| ORD ID | ord-c2943da7f39141e6b58dde35ea31a602 |
| Source note | uspto-grants-1998_07 |