HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 923659Generated: October 26, 2026
Tetrahydrofuran → 4-Bromo-6-[2-[tris(propan-2-yl)silyl]ethynyl}pyridin-2-amine
https://huagongshe.com/reaction/923659
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (Triisopropylsilyl)acetylene | HCID 2734682 | — |
| Reactant | 4,6-Dibromopyridin-2-amine | HCID 53440006 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 4-Bromo-6-[2-[tris(propan-2-yl)silyl]ethynyl}pyridin-2-amine | HCID 123389078 | — |
Reaction Steps
Under argon atmosphere dichlorobis(triphenylphosphine)palladium(II) (1.6 g, 2.2 mmol) is added to a mixture of 2-amino-4,6-dibromopyridine (5.44 g, 21.6 mmol), ethynyl-tri(propan-2-yl)silane (5.1 g, 28.1 mmol), copper(I) iodide (0.44 g, 2.3 mmol) and triethylamine (9 ml, 64 mmol) in ACN (32 ml) with THF (16 ml). After stirring at 50° C. for 17 h the mixture is diluted with water and extracted with EtOAc. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by NP chromatography. Yield: 4.7 g (62%). HPLC-MS: M+H=353/355; tR=1.80 min (METHOD—1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09278978B2 |
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| Source dataset | uspto-grants-2016_03 |
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| ORD ID | ord-c8c290959038463abdda31a65883c50f |
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| Source note | uspto-grants-2016_03 |
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