HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 630442Generated: October 30, 2026
Potassium Carbonate → (1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanone
https://huagongshe.com/reaction/630442
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Fluorophenylboronic acid | HCID 2734354 | — |
| Reactant | Tri-tert-butylphosphine tetrafluoroborate | HCID 2734635 | — |
| Reactant | (1-(5-Bromopyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanone | HCID 118666053 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Oxolane--water (1/1) | HCID 21881883 | — |
| Product | (1-(5-(2-Fluorophenyl)pyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)methanone | HCID 118666168 | — |
Reaction Steps
Potassium carbonate (5.73 g, 41.57 mmol, 3.0 eq), Pd2(dba)3 (1.26 g, 1.39 mmol, 0.1 eq) and tri-tert-butyl phosphonium tetrafluoroborate (0.2 g, 0.69 mmol, 0.05 eq) were added at room temperature under an argon atmosphere to a stirred solution of (1-(5-bromopyrimidin-2-yl)-3-(methylthio)-1H-indol-6-yl)(morpholino)-methanone (6.0 g, 13.85 mmol, 1.0 eq) and (2-fluorophenyl)boronic acid (2.31 g, 16.62 mmol, 1.2 eq) in THF/water (100 mL, 4:1). The mixture was stirred for 2 h at 30° C., diluted with ethyl acetate (50 mL), and filtered through a pad of celite. The filtrate was washed with water, dried over sodium sulphate and evaporated. The residue was purified by column chromatography [100-200 mesh; ethyl acetate/petrolether=2:3]. Yield: 4.0 g (64% of theory).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09315490B2 |
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| Source dataset | uspto-grants-2016_04 |
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| ORD ID | ord-d65d15d98f71450ebf287597410efd5c |
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| Source note | uspto-grants-2016_04 |
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