HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2297106Generated: October 27, 2026
Dimethylformamide dimethyl acetal → Ethyl 4-(4-cyanophenyl)-2-{[2-(2-quinolylamino)ethyl]amino}pyrimidine-5-carboxylate
https://huagongshe.com/reaction/2297106
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide dimethyl acetal | HCID 78373 | — |
| Reactant | Sodium ethoxide | HCID 2723922 | — |
| Reactant | Ethyl 3-(4-Cyanophenyl)-3-oxopropionate | HCID 2757969 | — |
| Reactant | 4-(2-{[2-(2-Quinolylamino)ethyl]amino}pyrimidin-4-yl)benzamide | HCID 22170111 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl 4-(4-cyanophenyl)-2-{[2-(2-quinolylamino)ethyl]amino}pyrimidine-5-carboxylate | HCID 22170113 | — |
Reaction Steps
Ethyl 3-(4-cyanophenyl)3-oxopropanoate (64 mg, 0.3 mmol) was heated with DMFDMA (50 μl) and dry THF (1 ml) at 70° C. for 3 hours. The cooled mixture was then added to a suspension of amino[2-(2-quinolylamino)ethyl]carboxamidinium 4-methylbenzenesulfonate (prepared according to Example 12), (120 mg, 0.3 mmol) in ethanol (2 ml) containing 0.35 mmol of sodium ethoxide. The reaction was then heated at 80° C. overnight and then concentrated in vacuo. The residue was taken up in dichloromethane and washed with saturated aqueous sodium bicarbonate. The organic layer was concentrated in vacuo. The residue was taken up in acetonitrile. Addition of water gave a precipitate which was filtered off and dried to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06489344B1 |
|---|
| Source dataset | uspto-grants-2002_12 |
|---|
| ORD ID | ord-96ce9940e3874298990974d779ed9798 |
|---|
| Source note | uspto-grants-2002_12 |
|---|