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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60173Generated: October 28, 2026

HCID 118874980, compound → 3-(6-(4-chlorophenyl)-5-isopentyl-1-methyl-2,4-dioxo-1,2-dihydropyrido[3,4-d]pyrimidin-3(4H)-yl)propyl formate

https://huagongshe.com/reaction/60173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 118874980HCID 118874980—
ReactantHCID 118874985HCID 118874985—
CatalystManganese dioxideHCID 14801—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(6-(4-chlorophenyl)-5-isopentyl-1-methyl-2,4-dioxo-1,2-dihydropyrido[3,4-d]pyrimidin-3(4H)-yl)propyl formateHCID 11887531166.7%

Reaction Steps

To a solution of 3-(6-(3-chlorophenyl)-5-isopentyl-1-methyl-2,4-dioxo-1,2-dihydropyrido[3,4-d]pyrimidin-3(4H)-yl)propyl formate and 3-(6-(3-chlorophenyl)-5-isopentyl-1-methyl-2,4-dioxo-1,2,7,8-tetrahydropyrido[3,4-d]pyrimidin-3(4H)-yl)propyl formate (21 mg, 0.047 mmol) in DCM (1 mL) was added MnO2 (40.8 mg, 0.47 mmol). The reaction was stirred at RT for 3 h then diluted with DCM (5 mL) and water (1 mL). The organic layer was washed with brine (1 mL), dried over Na2SO4, and concentrated to give 3-(6-(4-chlorophenyl)-5-isopentyl-1-methyl-2,4-dioxo-1,2-dihydropyrido[3,4-d]pyrimidin-3(4H)-yl)propyl formate (14 mg, 66.7% yield) as an oil. LCMS: MH+ 444 and TR=1.942 min. Used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440973B2
Source datasetuspto-grants-2016_09
ORD IDord-0474dd6e1629483c92688c593d790200
Source noteuspto-grants-2016_09