HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 269080Generated: October 31, 2026
Potassium Carbonate → 5-Ethynylpyridin-2-amine
https://huagongshe.com/reaction/269080
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 5-(2-(Trimethylsilyl)ethynyl)pyridin-2-amine | HCID 22482858 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-Ethynylpyridin-2-amine | HCID 21954827 | 73.2% |
Reaction Steps
To a solution of 5-trimethylsilanylethynyl-pyridin-2-ylamine (example D.1 method 1 step 1) (32.08 g, 169 mmol) in THF (150 mL) and MeOH (350 mL) at 0° C. was added K2CO3 (2.33 g, 10 mol %) and the mixture was stirred at 0° C. for 5 h. Diluted with ice water (500 mL), extracted with TBME (3×500 mL), washed the combined organic layers with brine, dried over MgSO4. Removal of the solvent in vacuum left a dark brown solid, which was dissolved in hot ethyl acetate and precipitated with n-heptane trituration to give the 5-ethynyl-pyridin-2-ylamine (14.61 g, 73%) as a light brown solid. Evaporation of the mother liquor followed by silica gel column chromatography gave a brown solid which was triturated with ether and n-heptane to give a second crop of the title compound (3.26 g, 16%) as a light brown solid. MS (EI) 118.1 [(M)+]; mp 143° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07446113B2 |
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| Source dataset | uspto-grants-2008_11 |
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| ORD ID | ord-3619fa69df394bd9868631a0e88b72ad |
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| Source note | uspto-grants-2008_11 |
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