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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | N-Methyl-5,6-diphenylpyrazin-2-amine | HCID 12548150 | — |
| Reactant | 5-(Benzyloxy)-2-(chloromethyl)-3,4-dihydronaphthalene | HCID 22932029 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(benzyloxy)-2-{[N-(5,6-diphenylpyrazin-2-yl)-N-methylamino]methyl}-3,4-dihydronaphthalene | HCID 18452657 | 104.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07205302B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-7b023f3a3ff949f9a0f0f2fa3d5faf74 |
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| Source note | uspto-grants-2007_04 |
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