HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 2-Methoxy-4-[(4-methylpiperazin-1-yl)methyl]benzoic acid methyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | Methyl 4-(bromomethyl)-2-methoxybenzoate | HCID 11288398 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Methoxy-4-[(4-methylpiperazin-1-yl)methyl]benzoic acid methyl ester | HCID 117888924 | 85% |
Reaction Steps
To 100 mL of ethanol were added 10.0 g of 1-methylpiperazine and 20.2 g of triethylamine. To the mixture cooled with ice, 25 mL of a solution of 24.6 g of 4-(bromomethyl)-2-methoxy-benzoic acid methyl ester in ethanol was added dropwise. The mixture was stirred at room temperature for 18 hours. The reaction mixture was concentrated. To the residue, 75 mL of water and 250 mL of methylene chloride were added, and the organic layer was separated. The obtained organic layer was dried over Na2SO4 and concentrated. The residue was purified by amino-silica gel column chromatography (heptane/AcOEt system) to give 22.4 g of the title compound (85% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09321752B2 |
| Source dataset | uspto-grants-2016_04 |
| ORD ID | ord-ee31b6255db64fbd9a3ebe8ab054d666 |
| Source note | uspto-grants-2016_04 |