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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 230124Generated: October 25, 2026

Aminopyrazine → 2-(4-(3-(1-(Hydroxyimino)-2,3-dihydro-1h-inden-5-ylamino)imidazo[1,2-a]pyrazin-2-yl)phenoxy)-n-methylacetamide

https://huagongshe.com/reaction/230124

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAminopyrazineHCID 78747—
Reactant2-(4-formylphenoxy)-N-methylacetamideHCID 15270519—
Reactant5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oximeHCID 57762062—
CatalystScandium(III) triflateHCID 2734571—
SolventDichloromethane methanolHCID 21226129—
Product2-(4-(3-(1-(Hydroxyimino)-2,3-dihydro-1h-inden-5-ylamino)imidazo[1,2-a]pyrazin-2-yl)phenoxy)-n-methylacetamideHCID 137194567—

Reaction Steps

A mixture of pyrazin-2-amine (12) (1.1 eq.), 2-(4-formylphenoxy)-N-methylacetamide (9) (1.1 eq.) and a catalytic amount of Sc(OTf)3 was stirred in 2 mL of 1:1 DCM/MeOH at room temperature for 30 minutes. To this was added 5-isocyano-2,3-dihydroinden-1-one O-tert-butyldimethylsilyl oxime (1 eq.) as a 2 mL solution in 1:1 DCM/MeOH and the mixture was stirred at room temperature for 18 hours. The reaction mixture was then concentrated under vacuum and the residue taken up in EtOAc (with a small amount of methanol added to help with dissolution) and purified by column using 1-5% MeOH/EtOAc+1% NH4OH. The desired product (14) was isolated as a light yellow solid. MS (APCI) m/z 443.1 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07566716B2
Source datasetuspto-grants-2009_07
ORD IDord-96fcc8a891764c2cbf2c88da8dd3c11d
Source noteuspto-grants-2009_07