HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526241Generated: November 4, 2026
2-Bromoethyl methyl ether → HCID 117667193, compound
https://huagongshe.com/reaction/1526241
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromoethyl methyl ether | HCID 80972 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 117667074 | HCID 117667074 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 117667193 | HCID 117667193 | — |
Reaction Steps
To a mixture of 5-chloro-6-ethyl-3-{[1-(piperidin-4-yl)-1H-pyrazol-4-yl]amino}pyrazine-2-carboxamide (350 mg), diisopropylethylamine (685 μL), and N,N-dimethylformamide (3.5 mL) was added 2-bromoethylmethyl ether (282 μL), followed by reacting at 60° C. for 2 hours. The mixture was subjected to liquid separation by the addition of ethyl acetate and a saturated aqueous sodium hydrogen carbonate solution. The organic phase was washed with saturated brine and dried over anhydrous sodium sulfate, and then the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (eluent; chloroform:methanol=99:1-90:10) to obtain 5-chloro-6-ethyl-3-({1-[1-(2-methoxyethyl)piperidin-4-yl]-1H-pyrazol-4-yl}amino)pyrazine-2-carboxamide (225 mg) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085540B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-ff910a9bf2784c6597993e8a2494c020 |
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| Source note | uspto-grants-2015_07 |
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