HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Aminoquinoline → (2-Chloropyrimidin-4-yl)quinolin-3-ylamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Aminoquinoline | HCID 11375 | — |
| Reactant | 2,4-Dichloropyrimidine | HCID 77531 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | (2-Chloropyrimidin-4-yl)quinolin-3-ylamine | HCID 22326846 | 68.7% |
Reaction Steps
50 g (0.34 mol) of 2,4-dichloropyrimidine and 50 g (0.35 mol) of 3-amino-quinoline are combined and kept at the boil under reflux for 50 h in 400 ml of 2-propanol with 100 ml of ethyldiisopropylamine. The reaction mixture is poured into 3 l of ice-water, the precipitate is filtered off with suction and washed with water. The residue is recrystallised from acetone, giving 60 g of pale-grey crystals (m.p.: 140-143° C.) (2-chloropyrimidin-4-yl)quinolin-3-ylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08114882B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-4fa377dae9a74f378f1d129a4b7490a4 |
| Source note | uspto-grants-2012_02 |