Back
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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromoethyl methyl etherHCID 80972—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 117667074HCID 117667074—
SolventDimethylformamideHCID 6228—
ProductHCID 117667193HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085540B2
Source datasetuspto-grants-2015_07
ORD IDord-ff910a9bf2784c6597993e8a2494c020
Source noteuspto-grants-2015_07