HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroquinone → 2-(2-chloro-5-methoxy-4-nitrophenyl)-N-(4-(4-methylpiperazin-1-yl)benzyl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroquinone | HCID 785 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | [4-(4-Methylpiperazin-1-yl)phenyl]methanamine | HCID 2776493 | — |
| Reactant | 1-Chloro-4-methoxy-5-nitro-2-vinylbenzene | HCID 67465947 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 2-(2-chloro-5-methoxy-4-nitrophenyl)-N-(4-(4-methylpiperazin-1-yl)benzyl)ethanamine | HCID 67465978 | 43% |
Reaction Steps
A mixture of 1-chloro-4-methoxy-5-nitro-2-vinylbenzene (0.42 g, 1.95 mmol), 4-(4-methyl-piperazin-1-yl)-benzylamine (1.2 g, 5.85 mmol) and quinol (0.043 g, 0.39 mmol) in n-butanol (8 mL) was heated to reflux for 12 hours under a N2 atmosphere. Water (100 mL) was added and the reaction mixture extracted with EtOAc (3×100 mL). The combined organic extracts were washed with brine (50 mL), dried (Na2SO4) and concentrated under reduced pressure. The residue was purified by column chromatography on neutral silica gel using 3-5% methanol in DCM to give the title compound (0.35 g, 43%) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08716287B2 |
| Source dataset | uspto-grants-2014_05 |
| ORD ID | ord-5e344b53b38647c18371b876261e3489 |
| Source note | uspto-grants-2014_05 |