HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → Methyl 2-(3-(piperazin-1-ylmethyl)phenyl)benzo[d]oxazole-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Methyl 2-(3-(bromomethyl)phenyl)benzo[d]oxazole-7-carboxylate | HCID 66620978 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Methyl 2-(3-(piperazin-1-ylmethyl)phenyl)benzo[d]oxazole-7-carboxylate | HCID 66621178 | 112.4% |
Reaction Steps
Methyl 2-(3-(bromomethyl)phenyl)benzo[d]oxazole-7-carboxylate (70 mg, 0.2 mmol) and piperazine (68.8 mg, 0.8 mmol) were added to ethanol (30 mL) and the mixture was stirred at room temperature for 1 hr. The resulting mixture was evaporated under reduced pressure to obtain methyl 2-(3-(piperazin-1-ylmethyl)phenyl)benzo[d]oxazole-7-carboxylate (79 mg, yield 91%). LC-MS (ESI) m/z 354 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088760B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-77b7bc414d3c4fc3bec45f75e09ba026 |
| Source note | uspto-grants-2012_01 |