HuagongsheHuagongshe Chemistry Print Report · For research reference only
N4-(3-bromophenyl)-4,6,7-Quinazolinetriamine → N-(3-bromophenyl)pyrazino[2,3-g]quinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N4-(3-bromophenyl)-4,6,7-Quinazolinetriamine | HCID 2426 | — |
| Reactant | 1,4-Dioxane-2,3-diol | HCID 96170 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | N-(3-bromophenyl)pyrazino[2,3-g]quinazolin-4-amine | HCID 5328246 | 84.1% |
Reaction Steps
A mixture of 4-(3-bromoanilino)-6,7-diaminoquinazoline (90 mg, 0.27 mmol) and 1,4-dioxane-2,3-diol (0.2 g, 1.6 mmol) [Venuti, M. C.; Synthesis, 1982, 61-63] in MeOH (20 mL) is stirred at room temperature overnight to give a precipitate of 4-(3-bromoanilino)pyrazino[2,3-g]quinazoline (80 mg, 83%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06596726B1 |
| Source dataset | uspto-grants-2003_07 |
| ORD ID | ord-9bc38be78ea04612aa042065386db123 |
| Source note | uspto-grants-2003_07 |