HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 592329Generated: October 31, 2026
Dimethylformamide → Methy 6-amino-4'-fluoro-5-[(2-hydroxy-2-methylpropyl)amino]biphenyl-3-carboxylate
https://huagongshe.com/reaction/592329
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Diisopropylamine | HCID 7912 | — |
| Reactant | 4-Fluorophenylboronic acid | HCID 285645 | — |
| Reactant | Methy 4-amino-3-bromo-5-[(2-hydroxy-2-methylpropyl)amino]benzoate | HCID 66693821 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 4,4',4''-Phosphinetriyltribenzenesulfonic acid sodium | HCID 131734552 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methy 6-amino-4'-fluoro-5-[(2-hydroxy-2-methylpropyl)amino]biphenyl-3-carboxylate | HCID 66693327 | 70.1% |
Reaction Steps
To a mixture of methy 4-amino-3-bromo-5-[(2-hydroxy-2-methylpropyl)amino]benzoate (513 mg, 1.617 mmol), palladium(II) acetate (7.26 mg, 0.032 mmol), (4-fluorophenyl)boronic acid (453 mg, 3.23 mmol) and 4,4′,4″-phosphinetriyltribenzenesulfonic acid-sodium salt (48.8 mg, 0.097 mmol) were added DMF (2.43 mL) and water (0.809 mL) followed by diisopropylamine (0.461 mL, 3.23 mmol). The reaction was capped and heated at 80° C. for 2 h. The reaction was cooled, quenched with saturated sodium bicarbonate and diluted with EtOAc. The aqueous layers were washed with EtOAc (2×) and the combined organics were washed with water (3×) and brine (1×). Organics were dried over magnesium sulfate, filtered and concentrated. Purification by reverse phase HPLC (C-18, 95% water/acetonitrile→5% water/acetonitrile with 0.1% TFA) gave the title compound (377 mg): LC-MS [M+1]=333.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09238647B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-e8f7bc8eed9a44e7a52b71be25df9a72 |
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| Source note | uspto-grants-2016_01 |
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