HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1029019Generated: October 31, 2026
Dichloromethane → 2-Amino-7-fluoro-3-morpholinoquinolin-6-ylboronic acid
https://huagongshe.com/reaction/1029019
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | Bis(pinacolato)diborane | HCID 2733548 | — |
| Reactant | 6-Bromo-7-fluoro-3-morpholinoquinolin-2-amine | HCID 71253124 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-Amino-7-fluoro-3-morpholinoquinolin-6-ylboronic acid | HCID 71253574 | — |
Reaction Steps
A microwave vessel was charged with potassium acetate (0.34 g, 3.46 mmol), [1,1′-bis(dppf)]dichloropalladium(II) complex with CH2Cl2 (0.038 g, 0.052 mmol), 4,4,4′,4′,5,5,5′,5′-octamethyl-2,2′-bi(1,3,2-dioxaborolane) (0.211 g, 0.831 mmol), 6-bromo-7-fluoro-3-morpholinoquinolin-2-amine (0.226 g, 0.693 mmol), and DMF (2.2 mL). The vessel was purged with argon, sealed, and heated by microwave radiation for 30 min at 125° C. The reaction was diluted with EtOAc (10 mL), and the suspension was filtered through celite rinsing with EtOAc. The filtrate was concentrated. The residue was purified by column chromatography on silica gel (25 mL) which had been deactivated with Et3N (2.5 mL) using 3% MeOH/DCM to afford 2-amino-7-fluoro-3-morpholinoquinolin-6-ylboronic acid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735384B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-4868332f76a845a280925b63c4d63bbf |
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| Source note | uspto-grants-2014_05 |
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