HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264777Generated: November 3, 2026
Potassium Acetate → 3-[3-Amino-1-(4-fluoro-3-pyrimidin-5-ylphenyl)-1H-isoindol-1-yl]phenyl trifluoromethanesulfonate
https://huagongshe.com/reaction/2264777
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 1,2-Dimethoxyethene | HCID 522390 | — |
| Reactant | (Pyrimidin-5-yl)boronic acid | HCID 2795193 | — |
| Reactant | 3-(3-Amino-1-(3-bromo-4-fluorophenyl)-1H-isoindol-1-yl)phenyl trifluoromethanesulfonate | HCID 59596268 | — |
| Catalyst | HCID 178418807 | HCID 178418807 | — |
| Solvent | Water | HCID 962 | — |
| Product | 3-[3-Amino-1-(4-fluoro-3-pyrimidin-5-ylphenyl)-1H-isoindol-1-yl]phenyl trifluoromethanesulfonate | HCID 24874865 | 37% |
Reaction Steps
3-(3-Amino-1-(3-bromo-4-fluorophenyl)-1H-isoindol-1-yl)phenyl trifluoromethane-sulfonate (Scheme #20, H, 0.083 g, 0.16 mmol), 5-pyrimidinylboronic acid (0.019 g, 0.16 mmol), potassium acetate (0.031 g, 0.31 mmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium(II) dichloride dichloromethane (0.006 g, 7.84 μmol) and solvent (2 mL of a mixture of dimethoxyethene and water in a ratio of 4:1) was irradiated under argon atmosphere in a microwave at 130° C. for 20 minutes. When cooled to ambient temperature the mixture was partitioned between ethylacetate and water, the organic phase was dried over magnesium sulfate and evaporated. Purification by preparative HPLC afforded 0.031 g (37%) of the title compound. 1H NMR (CDCl3) δ 9.18 (s, 1 H), 8.86 (d, J=1.26 Hz, 2 H), 7.58-7.45 (m, 4 H), 7.43-7.31 (m, 4 H), 7.30-7.25 (m, 1 H), 7.19-7.10 (m, 2 H), 5.43 (br s, 2 H); MS (ES) m/z 529 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07855213B2 |
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| Source dataset | uspto-grants-2010_12 |
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| ORD ID | ord-5c27961f69ab4d31adb49803c6c6e45a |
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| Source note | uspto-grants-2010_12 |
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