HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 1-(2-(5-Bromo-4-(thieno[2,3-c]pyridin-2-yl)pyrimidin-2-ylamino)ethyl)-5,5-dimethylimidazolidine-2,4-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-(2-Aminoethyl)-5,5-dimethylimidazolidine-2,4-dione | HCID 57428804 | — |
| Reactant | 2-(5-Bromo-2-chloropyrimidin-4-yl)thieno[2,3-c]pyridine | HCID 57428872 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 1-(2-(5-Bromo-4-(thieno[2,3-c]pyridin-2-yl)pyrimidin-2-ylamino)ethyl)-5,5-dimethylimidazolidine-2,4-dione | HCID 60204626 | — |
Reaction Conditions
| Temperature | 170 °C |
|---|
Reaction Steps
2-(5-Bromo-2-chloropyrimidin-4-yl)thieno[2,3-c]pyridine (0.38 g, 1.16 mmol), 1-(2-aminoethyl)-5,5-dimethylimidazolidine-2,4-dione (0.393 g, 2.3 mmol), diisopropylethyl-amine (0.4 mL, 2.3 mmol) and isopropyl alcohol (2 mL) were all placed in a microwave tube and heated to 170° C. for 20 min. The volatiles were removed in vacuo and the residue dissolved in 9:1 mixture of dichloromethane, preadsorbed onto silica gel and purified by flash chromatography using a gradient of 0 to 10% methanol in dichloromethane to obtain a yellow solid. Yield=0.4 g. MS (M+H)+ 461/463.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858785B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-25d14820cfcc4d858509282dddf2e4bc |
| Source note | uspto-grants-2010_12 |