HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → Ethanol, 2-[[2-amino-5-[(4-chlorophenyl)ethynyl]-4-pyrimidinyl]amino]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | 4-Chloro-5-(4-chlorophenylethynyl)-2-diisopropylaminomethyleneaminopyrimidine | HCID 73446449 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethanol, 2-[[2-amino-5-[(4-chlorophenyl)ethynyl]-4-pyrimidinyl]amino]- | HCID 9857143 | — |
Reaction Steps
A mixture of 0.7 g of 4-chloro-5-(4-chlorophenylethynyl)-2-diisopropylaminomethyleneamino-pyrimidine, 20 mL ethanol and 0.6 mL ethanolamine was refluxed for 18 hours. The green solution was evaporated in vacuo and triturated with water. The insoluble yellow residue was recrystallized by dissolving in 35 mL hot methanol, concentrating to 10 mL and chilling. The pale yellow powdery precipitate was filtered and dried to yield 0.34 g of 2-amino-5-(4-chlorophenylethynyl)-4-(2-hyroxyethylamino)pyrimidine, m.p. 197–200° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07205297B2 |
| Source dataset | uspto-grants-2007_04 |
| ORD ID | ord-89b0b7b6b2dc4ca7aec700dedbfebed3 |
| Source note | uspto-grants-2007_04 |