HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(4-Aminophenyl)ethylamine → N-(4-aminophenethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(4-Aminophenyl)ethylamine | HCID 72895 | — |
| Reactant | 4-Chloro-5,6-diphenylfuro[2,3-d]pyrimidine | HCID 11449637 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | N-(4-aminophenethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-4-amine | HCID 46855043 | 74% |
Reaction Steps
4-Chloro-5,6-diphenylfuro[2,3-d]pyrimidine (0.200 g) and 4-(2-aminoethyl)aniline (0.107 g) in n-butanol (5 mL) were heated at 80° C. for 16 h. The reaction mixture was concentrated and the residue was partitioned between water and ethyl acetate. The organic layer was concentrated and the crude compound was purified by silica gel column chromatography using a mixture of dichloromethane:methanol (40:1), to give N-(4-aminophenethyl)-5,6-diphenylfuro[2,3-d]pyrimidin-4-amine (0.195 g, 74%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08138194B2 |
| Source dataset | uspto-grants-2012_03 |
| ORD ID | ord-df27339b0eb54779996fe49ae54f0d63 |
| Source note | uspto-grants-2012_03 |