HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → 5-Amino-2-bromo-6-fluoro-4-methoxybiphenyl-3-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 5-Amino-6-fluoro-4-methoxybiphenyl-3-carbonitrile | HCID 86097506 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 5-Amino-2-bromo-6-fluoro-4-methoxybiphenyl-3-carbonitrile | HCID 86097508 | 89.5% |
Reaction Steps
5-Amino-6-fluoro-4-methoxybiphenyl-3-carbonitrile (I-234) (500 mg, 2.06 mmol) was dissolved in acetic acid (9.5 ml), and at room temperature, N-bromosuccinimide (441 mg, 2.48 mmol) was gradually added. After stirring under nitrogen atmosphere at room temperature for 1 hour, the solvent was evaporated away under reduced pressure. The residue was fractionated with ethyl acetate and aqueous 1M sodium hydroxide solution. The organic layer was washed with saturated brine, and dried over anhydrous sodium sulfate. After filtration, the solvent was evaporated away, and the resulting residue was purified by middle-pressure liquid chromatography (eluent, hexane:ethyl acetate=3:1) to obtain the entitled compound (592 mg, 89%) as a pale brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737166B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-618182d5fd9d4d75b4fee67d0e8f90e2 |
| Source note | uspto-grants-2010_06 |