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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 1H-Indazol-5-amine | HCID 88012 | — |
| Reactant | 2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one | HCID 89570391 | — |
| Solvent | 2,2,2-Trifluoroethanol | HCID 6409 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-(1H-indazol-5-ylamino)-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one | HCID 89570390 | 40% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09351974B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-7683e10dacff440ebd552a20a52315eb |
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| Source note | uspto-grants-2016_05 |
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