HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446924Generated: October 30, 2026
Tetrabutylammonium Fluoride → N-[3-(1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenyl]-benzamide
https://huagongshe.com/reaction/446924
Participants
| Role | Name | HCID | Charge |
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| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 4-Bromo-1-methyl-1H-pyrazolo(3,4-c)pyridine | HCID 57606936 | — |
| Reactant | HCID 67399535 | HCID 67399535 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-[3-(1-Methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenyl]-benzamide | HCID 59536452 | — |
Reaction Steps
In an adaption of GP 3c, 60 mg of 4-bromo-1-methyl-1H-pyrazolo[3,4-c]pyridine (Intermediate 2.1, 0.28 mmol, 1 eq), 140 mg N-(3-trimethylsilanylethynyl-phenyl)-benzamide (0.48 mmol, 1.68 eq.), 10 mg dichlorobis(triphenylphosphine)palladium (II) (PdCl2(PPh3)2) (0.014 mmol, 5 mol %) and 10.8 mg copper (I) iodide (0.057 mmol, 0.2 eq.) were dissolved in 1.4 mL THF (0.2 M) and treated with 0.35 mL tetra-n-butylammonium fluoride solution (1.0 M in THF, 0.35 mmol, 1.25 eq.). The resulting mixture was heated to 80° C. in a Biotage Initiator microwave oven for 30 min. Extractive work-up followed by column chromatography and preparative HPLC purification provided the target compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481539B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-4356746b20724ab586c8f0354645e551 |
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| Source note | uspto-grants-2013_07 |
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