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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1037682Generated: October 30, 2026

4-Methylmorpholine → {2-Amino-6-[2-(4-methylpiperazine-1-carbonyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanone

https://huagongshe.com/reaction/1037682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantPyrrolidineHCID 31268—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant2-[2-Amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzoic acidHCID 58457191—
SolventDimethylformamideHCID 6228—
Product{2-Amino-6-[2-(4-methylpiperazine-1-carbonyl)phenyl]quinazolin-4-yl}-(1,3-dihydroisoindol-2-yl)methanoneHCID 46701159—

Reaction Conditions

Temperature25 °C

Reaction Steps

175.9 mg of O-(benzotriazol-1-yl)-N,N,N′,N′-tetramethyluronium tetrafluoroborate (TBTU), 33.8 μl of pyrrolidine and 200.9 μl of 4-methylmorpholine are added to a solution of 150 mg of 2-[2-amino-4-(1,3-dihydroisoindole-2-carbonyl)quinazolin-6-yl]benzoic acid in 1 ml of dimethylformamide. The mixture is subsequently stirred at 25° C. for 12 h. The mixture is evaporated to dryness in vacuo, the residue is taken up in 1 ml of dimethyl sulfoxide and purified by chromatography (reversed phase HPLC).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08546565B2
Source datasetuspto-grants-2013_10
ORD IDord-f54c5ad49e014392a4085eabc77f567e
Source noteuspto-grants-2013_10