HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropanol → 6-Chloro-4-[(propan-2-yl)oxy]pyrido[3,2-d]pyrimidin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | 6-Chloro-4-(1H-1,2,4-triazol-1-yl)pyrido[3,2-d]pyrimidin-2-amine | HCID 57698314 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-Chloro-4-[(propan-2-yl)oxy]pyrido[3,2-d]pyrimidin-2-amine | HCID 58019801 | 67% |
Reaction Steps
Potassium tert-butoxide (4.0 mL; 1M in THF) was added to a suspension of 6-chloro-4-[1,2,4]triazol-1-yl-pyrido[3,2-d]pyrimidin-2-ylamine (1.0 g) and 2-propanol (0.313 mL) in DCM (50 mL). After stirring at room temperature for 30 minutes, the mixture was diluted with DCM (100 mL) and washed with brine. The organic layer was dried over Na2SO4 and concentrated to afford 6-chloro-4-(2-propoxy)-pyrido[3,2-d]pyrimidin-2-ylamine as a yellow solid (0.65 g, yield: 67%) which was characterized by its mass spectrum as follows: MS (m/z) 239.1 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08143394B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-a22d3f1f7cbb4ad0a3dee6584612aa7f |
| Source note | uspto-grants-2012_03 |