HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Methyl 5-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]benzofuran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-(4-Pyridyl)piperazine | HCID 70517 | — |
| Reactant | Methyl 5-(2-bromoacetyl)benzofuran-2-carboxylate | HCID 18918450 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | Methyl 5-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]benzofuran-2-carboxylate | HCID 18918243 | — |
Reaction Steps
To a solution of 1-(4-pyridyl)piperazine (262 mg) and triethylamine (0.1 ml) in acetonitrile (10 ml) was added dropwise over 40 minutes a solution of methyl 5-(2-bromoacetyl)benzofuran-2-carboxylate in acetonitrile (5 ml). The resulting mixture was stirred for 2 hours, concentrated and purified by flash column chromatography on grade III alumina, eluting with methanol/dichloromethane (1:99 to 4:96 v/v) to give the title compound as a solid (138 mg); m.p. 173°-177° C., NMR 2.66(4H,m), 3.8(4H,m), 3.91(3H,s), 4.00(2H,s), 6.82(2H,m), 7.8°-8.5(6H,m); m/e 380 (M+H+); calculated for C21H21N3O4. 0.5H2O: C, 64.9; H, 5.7; N, 10.8. Found: C, 65.2; H, 5.7; N, 10.9%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05750754 |
| Source dataset | uspto-grants-1998_05 |
| ORD ID | ord-8b6d4034b48542dfb868a57df9983ab8 |
| Source note | uspto-grants-1998_05 |