HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 4-(2-Aminobenzylamino)-7-ethylamino-6-nitroquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Aminomethyl)aniline | HCID 178096 | — |
| Reactant | 4-Chloro-7-ethylamino-6-nitroquinazoline | HCID 23292989 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(2-Aminobenzylamino)-7-ethylamino-6-nitroquinazoline | HCID 23293013 | 78.1% |
Reaction Steps
4-Chloro-7-ethylamino-6-nitroquinazoline (5.00 g, 19.8 mmol), triethylamine (8.3 ml, 60.9 mmol), and 2-aminobenzylamine (2.9 g, 23.8 mmol) were stirred at room temperature overnight in tetrahydrofuran. After the reaction was completed, the solution was concentrated under reduced pressure, and the resulting solids were washed with methanol to give the title compound (5.23 g, 78%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06127541 |
| Source dataset | uspto-grants-2000_10 |
| ORD ID | ord-faac0658e24944a9adef8d8190e97f56 |
| Source note | uspto-grants-2000_10 |