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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469873Generated: October 29, 2026

2-Naphthalenecarboxaldehyde → 5-bromo-N-(naphthalen-2-ylmethyl)pyrazin-2-amine

https://huagongshe.com/reaction/469873

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-NaphthalenecarboxaldehydeHCID 6201—
Reactant2-Amino-5-bromopyrazineHCID 599539—
ReactantSodium triacetoxyborohydrideHCID 5049666—
SolventAcetic AcidHCID 176—
SolventDichloromethaneHCID 6344—
Solvent1,1-DichloroethaneHCID 6365—
Product5-bromo-N-(naphthalen-2-ylmethyl)pyrazin-2-amineHCID 8661430748.7%

Reaction Steps

2-Napthaldehyde (0.6 g, 3.84 mmol) and 2-amino-5-bromopyrazine (0.56 g, 3.201 mmol) were treated with Na(OAc)3BH (1.02 g, 4.802 mmol) in dichloroethane (15.0 mls) and acetic acid (0.5 mls) for 18 hours at room temperature. The mixture was diluted with dichloromethane, washed with 1.0 N NaOH, washed with brine, dried over MgSO4, and concentrated. Chromatography (SiO2, EtOAc:Hex, 1:1) gave 0.49 g 5-bromo-N-(naphthalen-2-ylmethyl)pyrazin-2-amine.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629156B2
Source datasetuspto-grants-2014_01
ORD IDord-719929ee8809478ca8284915f2a40447
Source noteuspto-grants-2014_01