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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 325608Generated: October 28, 2026

HCID 20463835, compound → 5,6-Dichloro-3-[(2-hydroxyethyl)amino]pyrazine-2-carbaldehyde

https://huagongshe.com/reaction/325608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20463835HCID 20463835—
CatalystHCID 178418406HCID 178418406—
SolventAcetoneHCID 180—
Product5,6-Dichloro-3-[(2-hydroxyethyl)amino]pyrazine-2-carbaldehydeHCID 2046383671.5%

Reaction Steps

A mixture of 5,6-dichloro-3-hydroxymethyl-2-(2-hydroxyethyl)aminopyrazine (38 mg; 0.00016 Mol), prepared as in Step C above, and manganese dioxide (12 mg) was stirred at room temperature for 2.5 hours. Another 24 mg of manganese dioxide was added and stirring was continued for another 5 hours. The manganese dioxide was filtered off, and the precipitate was washed well with acetone. The crude reaction mixture dissolved in 1.5 l of acetone and 36 mg of manganese dioxide was added, followed by stirring at room temperature for 3.5 hours. The manganese dioxide was filtered off, and the precipitate was washed twice with acetone. The filtrate was concentrated under vacuum and passed through a silica gel column, eluting with dichloromethane, then 1:1 ethyl acetate/dichloromethane, to give the title compound (27 mg). Elemental Analysis for C7H7O2N3Cl2 :

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04442097
Source datasetuspto-grants-1984_04
ORD IDord-a665aae9153149b080c5fd4e9e4a120a
Source noteuspto-grants-1984_04