HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Carbonate → 1-(2'-Fluoro-6-nitro-biphenyl-3-yl)-4-methyl-piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | 1-(3-Bromo-4-nitrophenyl)-4-methylpiperazine | HCID 11781541 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Solvent | Methylenechloride Hexane | HCID 21226440 | — |
| Product | 1-(2'-Fluoro-6-nitro-biphenyl-3-yl)-4-methyl-piperazine | HCID 59128564 | 120.5% |
Reaction Steps
The procedure of Example 9, step (b) was followed using 75.0 mg (0.250 mmol) 1-(3-bromo-4-nitro-phenyl)-4-methyl-piperazine (as prepared in Example 9, step (a)), 136 mg (0.999 mmol) 2-fluorophenylboronic acid, 26.8 mg (0.0232 mmol) of tetrakis(triphenylphosphine)palladium (0) and 400 μL (0.799 mmol) of 2.0 M aq Na2CO3 in DME except the mnixture was heated for 22 h. Chromatography on a 5-g silica SPE column with 1-5% MeOH in dichloromethane-hexane (1:1) afforded 95.0 mg of the title compound (76% purity by 1H-NMR as a mixture with triphenylphosphine) as a yellow resin that was used in the following reaction without further purification. Mass spectrum (ESI, m/z): Calcd. for C17H18FN3O3, 316.1 (M+H), found 316.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07645755B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-3f65f70a106444e5a02b236809d733b8 |
| Source note | uspto-grants-2010_01 |