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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517421Generated: October 30, 2026

p-Toluenesulfonic acid → HCID 68912489, compound

https://huagongshe.com/reaction/1517421

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantMorpholineHCID 8083—
ReactantHexamethyldisilazaneHCID 13838—
ReactantSodium ethoxideHCID 2723922—
ReactantAmmonium SulfateHCID 6097028—
ReactantHCID 136397030HCID 136397030—
SolventEthanolHCID 702—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductHCID 68912489HCID 6891248925%

Reaction Steps

to a suspension of 2-acetamido-6-(3-methyl-4-fluorophenyl)-pyrido[3,2-d]pyrimidin-4(3H)-one (312 mg, 1 mmol) in toluene (10 ml) was added morpholine (4 mmol, 0.23 ml), p-toluene sulfonic acid (0.1 mmol, 19 mg), ammonium sulfate (13 mg, 0.1 mmol) and 1,1,1,3,3,3-hexamethyldisilazane (2 ml, 8 mmol). The reaction mixture was refluxed for 48 hours till a brown solution was formed. The solvents were evaporated in vacuo, yielding crude 2-acetamido-4-(morpholino)-6-(4-methyl-3-fluoro-phenyl)-pyrido[3,2-d]pyrimidine. The residue was redissolved in a mixture of dichloromethane and ethanol (in a ratio of 80/20, 10 ml). A sodium ethoxide solution (0.2 N solution) was added till pH 12 and the resulting mixture was stirred overnight at room temperature. The solvents were evaporated in vacuo. The crude residue was purified by preparative TLC on silica, using a methanol/dichloromethane mixture in a ratio of 10:90 as mobile phase, yielding pure 2-amino-4-(morpholino)-6-(3-methyl-4-fluoro-phenyl)-pyrido[3,2-d]pyrimidine (80 mg, yield: 25%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08232278B2
Source datasetuspto-grants-2012_07
ORD IDord-f2f1d0f9af26479bacc386805154da6a
Source noteuspto-grants-2012_07