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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170928Generated: October 31, 2026

HCID 59553890, compound → 3-(1-(3,4-difluorophenyl)propan-2-yl)-2-(3-hydroxypyridin-2-yl)-5-(trifluoromethyl)pyrido[4,3-d]pyrimidin-4(3H)-one

https://huagongshe.com/reaction/1170928

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59553890HCID 59553890—
CatalystHCID 178418406HCID 178418406—
SolventMethyl Isobutyl KetoneHCID 7909—
Product3-(1-(3,4-difluorophenyl)propan-2-yl)-2-(3-hydroxypyridin-2-yl)-5-(trifluoromethyl)pyrido[4,3-d]pyrimidin-4(3H)-oneHCID 135948808—

Reaction Conditions

Temperature90 °C

Reaction Steps

3-(1-(3,4-difluorophenyl)propan-2-yl)-2-(3-hydroxypyridin-2-yl)-5-(trifluoromethyl)-2,3-dihydropyrido[4,3-d]pyrimidin-4(1H)-one (5.90 g, 12.7 mmol) was dissolved in 500 mL of 4-methyl-2-pentanone. To this solution, manganese dioxide was added (16.6 g, 191 mmol) and the mixture was heated to 90° C. for 1 hour. The reaction was cooled, filtered through Celite and washed with CH2CL2. The filtrate was collected and concentrated in vacuo as a yellow solid which was purified by silica gel chromatography to afford the racemic mixture 3-(1-(3,4-difluorophenyl)propan-2-yl)-2-(3-hydroxypyridin-2-yl)-5-(trifluoromethyl)pyrido[4,3-d]pyrimidin-4(3H)-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829572B2
Source datasetuspto-grants-2010_11
ORD IDord-be7f6bd3f1744c9fa47c00b385b9c53e
Source noteuspto-grants-2010_11