HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446922Generated: October 26, 2026
Tetrabutylammonium Fluoride → 4-Methyl-3-(1-methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenylamine
https://huagongshe.com/reaction/446922
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrabutylammonium Fluoride | HCID 2724141 | — |
| Reactant | 3-[2-(Trimethylsilyl)ethynyl]aniline | HCID 11159794 | — |
| Reactant | 4-Bromo-1-methyl-1H-pyrazolo(3,4-c)pyridine | HCID 57606936 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Methyl-3-(1-methyl-1H-pyrazolo[3,4-c]pyridin-4-ylethynyl)-phenylamine | HCID 59536437 | 58.5% |
Reaction Steps
In an adaption of GP 3c, 640 mg of 4-bromo-1-methyl-1H-pyrazolo[3,4-c]pyridine (Intermediate 2.1, 3 mmol, 1 eq), 1000 mg 3-trimethylsilanylethynyl-phenylamine (4.92 mmol, 1.63 eq.), 106 mg dichlorobis(triphenylphosphine)palladium (II) (PdCl2(PPh3)2) (0.15 mmol, 5 mol %) and 115 mg copper (I) iodide (0.6 mmol, 0.2 eq.) were dissolved in 15 mL THF (0.2 M) and treated with 3.6 mL tetra-n-butylammonium fluoride solution (1.0 M in THF, 3.6 mmol, 1.2 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 provided the 460 mg of the target compound (58% yield).
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-0f56cb9feb0a4d4cacf64708b2641f9a |
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| Source note | uspto-grants-2013_07 |
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