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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014702Generated: October 30, 2026

3-Methoxybenzylamine → HCID 136115967, compound

https://huagongshe.com/reaction/1014702

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-MethoxybenzylamineHCID 21156—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 86626396HCID 86626396—
ReactantHCID 86626397HCID 86626397—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 136115967HCID 13611596720%

Reaction Steps

7-Bromo-1-(3-methoxybenzyl)-3,4-dihydropyrazino[2,3-b]pyrazin-2(1H)-one. Methyl 2-(3,5-dibromopyrazin-2-ylamino)acetate (0.58 g, 1.8 mmol), 3-methoxybenzylamine (227 μL, 1.8 mmol), diisopropylethylamine (1 mL), and dimethylsulfoxide (1 mL) were heated to 100° C. for 3 d under nitrogen. The reaction was extracted with ethyl acetate and water. The organic layer was dried with magnesium sulfate, filtered and concentrated. The residue was purified on silica gel column (0-100% ethyl acetate in hexanes) to give the title compound (124 mg, 20% yield) as a pink solid. MS (ESI) m/z 349.0 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07981893B2
Source datasetuspto-grants-2011_07
ORD IDord-b846d2c0a040452b9ddbd0acb41e7693
Source noteuspto-grants-2011_07