HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408474Generated: October 29, 2026
Chloride → 2-(2,6-Difluorophenyl)-8-methoxyquinazoline
https://huagongshe.com/reaction/408474
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chloride | HCID 312 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,6-Difluorophenylboronic acid | HCID 2734336 | — |
| Reactant | 2-Chloro-8-methoxyquinazoline | HCID 19988695 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-(2,6-Difluorophenyl)-8-methoxyquinazoline | HCID 58386803 | — |
Reaction Steps
2-chloro-8-methoxyquinazoline (1.0 eq), 2,6-difluorophenylboronic acid (1.5 eq), and DIPEA (3 eq) was mixed with toluene and ethanol (1:1, 0.5M) in a microwave vial. The reaction mixture was degassed by anhydrous N2 stream for 5 min followed by the addition of Pd(dppf)Cl2-DCM (0.1 eq). The reaction mixture was stirred at 130° C. for 30 min in microwave. Solvents were removed under reduced pressure. The crude product was purified by column (ethyl acetate:hexanes=1:1) to give the mixture of starting material chloride and desired product. The mixture was treated with 1N HCl in 1,4-dioxane. Solvents were removed under reduced pressure. The residue was dissolved in ethyl acetate (150 mL), and washed with NaHCO3, brine, then dried over MgSO4, filtered, and evaporated under reduced pressure to give crude product, which was purified by column (ethyl acetate:hexanes=1:1) to yield 2-(2,6-difluorophenyl)-8-methoxyquinazoline (46%). LC/MS (m/z): 273.0 (MH+), Rt=0.78.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759338B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-52d06594b5f44f619c4684a1d851b1ed |
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| Source note | uspto-grants-2014_06 |
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