Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 467602Generated: October 26, 2026

Piperidine → 4-Piperidine-1-yl-but-2-enoic acid [4-(3-chloro-4-fluoro-phenylamino)-7-(2,2-difluoro-ethoxy)-quinazolin-6-yl]-amide

https://huagongshe.com/reaction/467602

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromo-but-2-enoyl chlorideHCID 53635200—
ReactantN4-(3-Chloro-4-fluoro-phenyl)-7-(2,2-difluoro-ethoxy)-quinazoline4,6-diamineHCID 86601522—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Piperidine-1-yl-but-2-enoic acid [4-(3-chloro-4-fluoro-phenylamino)-7-(2,2-difluoro-ethoxy)-quinazolin-6-yl]-amideHCID 73063630—

Reaction Steps

0.5 g N4-(3-Chloro-4-fluoro-phenyl)-7-(2,2-difluoro-ethoxy)-quinazoline-4,6-diamine was dissolved in 10 ml THF and 1.2 ml N,N-Diisopropyl-ethylamine (DIEA) and 0.48 g 4-Bromo-but-2-enoyl chloride were added and the mixture was stirred at room temperature for 2 hours. 0.27 ml piperidine was added and stirred at room temperature overnight. An additional 0.7 ml piperidine was added and the mixture heated to 70° C. After 3 hours the reaction mixture was poured into water, the solids were extracted with ethyl acetate, washed with water and brine, dried over NaSO4 and flash chromatographed under 0-4% methanol in chloroform to yield 0.2 g 4-Piperidine-1-yl-but-2-enoic acid [4-(3-chloro-4-fluoro-phenylamino)-7-(2,2-difluoro-ethoxy)-quinazolin-6-yl]-amide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08623883B2
Source datasetuspto-grants-2014_01
ORD IDord-18e9449a9f8b40f9bd9a08aece9335c4
Source noteuspto-grants-2014_01