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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1271295Generated: November 1, 2026

Sodium hydride → 5-(benzyloxy)-2-{[N-(5,6-diphenylpyrazin-2-yl)-N-methylamino]methyl}-3,4-dihydronaphthalene

https://huagongshe.com/reaction/1271295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantN-Methyl-5,6-diphenylpyrazin-2-amineHCID 12548150—
Reactant5-(Benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthaleneHCID 22932029—
SolventDimethylformamideHCID 6228—
Product5-(benzyloxy)-2-{[N-(5,6-diphenylpyrazin-2-yl)-N-methylamino]methyl}-3,4-dihydronaphthaleneHCID 18452657104.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under an argon atmospshere, 0.97 g of 60% sodium hydride was suspended in anhydrous N,N-dimethylformamide and 0.97 g of 5,6-diphenyl-2-(methylamino)-pyrazine was added in three portions. After stirring at 80° C. for 30 minutes, the reaction solution was ice-cooled and a solution of 0.97 g of 5-(benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthalene in 5 ml of anhydrous N,N-dimethylformamide was added dropwise. After stirring for 30 minutes, the reaction solution was diluted with ice water and then extracted with diethyl ether. The extract was washed with water and dried over anhydrous magnesium sulfate, and then the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography to obtain 1.81 g of the desired compound as a pale yellow amorphous.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07205302B2
Source datasetuspto-grants-2007_04
ORD IDord-7b023f3a3ff949f9a0f0f2fa3d5faf74
Source noteuspto-grants-2007_04