HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384642Generated: October 29, 2026
2-Amino-5-bromopyrazine → HCID 59613433, compound
https://huagongshe.com/reaction/384642
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Amino-5-bromopyrazine | HCID 599539 | — |
| Reactant | tert-Butyl(dimethyl)[(prop-2-yn-1-yl)oxy]silane | HCID 3445622 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Product | HCID 59613433 | HCID 59613433 | 91% |
Reaction Steps
2-Amino-5-bromopyrazine (1.50 g, 8.6 mmol) was dissolved in anhydrous, deoxygenated DMF (24.5 mL) with triethylamine (10.5 mL). Copper(I) iodide (0.33 g, 1.7 mmol), tetrakis(triphenylphosphine)-palladium(0) (0.61 g, 0.51 mmol) and tert-butyldimethyl(prop-2-ynyloxy)silane (1.90 g, 11.2 mmol) were added and the solution was stirred overnight at 60° C., then cooled and partitioned between water and dichloromethane. The aqueous phase was extracted with dichloromethane and the combined organic phases were dried (Na2SO4) and evaporated. The residue was purified by silica chromatography to give 2-amino-5-(3-(tert-butyldimethylsilyloxy)prop-1-ynyl)pyrazine (2.06 g, 91%) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367658B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-a9694d9ce95a4080ba633b35d4919f5c |
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| Source note | uspto-grants-2013_02 |
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