HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (2E)-4-bromo-N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-2-butenamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | (E)-4-Bromo-2-butenoyl Chloride | HCID 11263885 | — |
| Reactant | N4-(3-Chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamine | HCID 21847826 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (2E)-4-bromo-N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-2-butenamide | HCID 66823741 | 79% |
Reaction Steps
To a stirred solution of N4-(3-chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamine (8) (4.0 g, 12.5 mmol) in dry tetrahydrofuran (150 mL) under nitrogen was added triethylamine (19 mmol), followed by freshly prepared (2E)-4-bromo-2-butenoyl chloride (15 mmol) in dry tetrahydrofuran (50 mL). The resulting solution was then stirred at room temperature for 2 hours and concentrated under reduced pressure. Trituration from dichloromethane gave crude (2E)-4-bromo-N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-2-butenamide (4.6 g) that was used directly.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09073916B2 |
| Source dataset | uspto-grants-2015_07 |
| ORD ID | ord-2b8ccc428a684346a6b4e746da0f5c96 |
| Source note | uspto-grants-2015_07 |