HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1517421Generated: October 30, 2026
p-Toluenesulfonic acid → HCID 68912489, compound
https://huagongshe.com/reaction/1517421
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Hexamethyldisilazane | HCID 13838 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ammonium Sulfate | HCID 6097028 | — |
| Reactant | HCID 136397030 | HCID 136397030 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68912489 | HCID 68912489 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08232278B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-f2f1d0f9af26479bacc386805154da6a |
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| Source note | uspto-grants-2012_07 |
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