Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449016Generated: October 29, 2026

Nitrogen → 3-(4-Methoxyimidazo[5,1-f][1,2,4]triazin-7-yl)cyclobutanone

https://huagongshe.com/reaction/449016

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantAcetonitrileHCID 6342—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantN-[(5-methoxy-1,2,4-triazin-6-yl)methyl]-3-oxocyclobutanecarboxamideHCID 66915404—
SolventDimethylformamideHCID 6228—
Product3-(4-Methoxyimidazo[5,1-f][1,2,4]triazin-7-yl)cyclobutanoneHCID 66915595—

Reaction Steps

In an oven-dried flask filled with N2 was added N-[(5-methoxy-1,2,4-triazin-6-yl)methyl]-3-oxocyclobutanecarboxamide (2.40 g, 0.00833 mol) followed by MeCN (200 mL) and DMF (40 mL). The reaction mixture was treated with POCl3 (3.1 mL, 0.033 mol) dropwise at 0° C. under N2 over 10 min. The reaction was stirred at rt overnight. The reaction mixture was concentrated and poured into ice, saturated aqueous NaHCO3 solution was added to adjust the pH to 7. The mixture was extracted with DCM (150×3). The organic extracts were combined, dried (Na2SO4) and concentrated under reduced pressure to give a crude residue, which was then purified by flash chromatography on silica gel using hexanes:EtOAc (1:1) as the eluent.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481733B2
Source datasetuspto-grants-2013_07
ORD IDord-f2de9036ad8b43e8a7f9777ca4228c63
Source noteuspto-grants-2013_07