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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530112Generated: October 30, 2026

Trifluoroacetic acid → 2-(1H-indazol-5-ylamino)-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one

https://huagongshe.com/reaction/530112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant1H-Indazol-5-amineHCID 88012—
Reactant2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-oneHCID 89570391—
Solvent2,2,2-TrifluoroethanolHCID 6409—
SolventEthyl AcetateHCID 8857—
Product2-(1H-indazol-5-ylamino)-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-oneHCID 8957039040%

Reaction Conditions

Temperature125 °C

Reaction Steps

To a mixture of 2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one (175 mg, 0.5 mmol), 5-aminoindazole (99 mg, 0.75 mmol), in trifluoroethanol (2 mL) in a microwave reactor vial was added trifluoroacetic acid (171 mg). The vial was then sealed and heated in a microwave reactor at 125° C. for 30 minutes. The reaction mixture was then diluted with ethyl acetate (25 mL) and washed with aqueous saturated aq. sodium bicarbonate. The organic layer was dried (Na2SO4) and evaporated to give a crude material, which was then purified by silica gel column chromatography (eluent: 2% methanol in dichloromethane) to give the desired product (40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09351974B2
Source datasetuspto-grants-2016_05
ORD IDord-7683e10dacff440ebd552a20a52315eb
Source noteuspto-grants-2016_05