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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520727Generated: November 4, 2026

Triethylamine → (2E)-4-bromo-N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-2-butenamide

https://huagongshe.com/reaction/1520727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(E)-4-Bromo-2-butenoyl ChlorideHCID 11263885—
ReactantN4-(3-Chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamineHCID 21847826—
SolventTetrahydrofuranHCID 8028—
Product(2E)-4-bromo-N-[4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl]-2-butenamideHCID 6682374179%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073916B2
Source datasetuspto-grants-2015_07
ORD IDord-2b8ccc428a684346a6b4e746da0f5c96
Source noteuspto-grants-2015_07