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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 394740생성일: 2026년 10월 25일

Acrylic Acid → N-[4-(3-Bromo-phenylamino)-7-(4-dimethylamino-butoxy)-quinazolin-6-yl]-acrylamide

https://huagongshe.com/reaction/394740

반응식

참여 물질

역할이름HCID투입량
반응물Acrylic AcidHCID 6581—
반응물TriethylamineHCID 8471—
반응물1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
반응물6-amino-4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]quinazolineHCID 10693912—
용매DimethylacetamideHCID 31374—
용매Ethyl acetate hexaneHCID 21226206—
용매Ethylacetate methanolHCID 21584119—
용매Ethyl ether methylene chlorideHCID 21881112—
생성물N-[4-(3-Bromo-phenylamino)-7-(4-dimethylamino-butoxy)-quinazolin-6-yl]-acrylamideHCID 1060088832%

반응 단계

To a stirred solution of the above 6-aminoquinazoline (276 mg, 0.64 mmol), acrylic acid (6 mol eq., 3.85 mmol, 264 mL), and Et3N (excess, 1.0 mL) in DMA (10 mL) under N2 was added 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDCI.HCl) (3 mol eq., 1.92 mmol, 369 mg). The standard procedure above was followed to give after chromatography on grade III alumina eluting with EtOAc/hexane (1:1) to MeOH/EtOAc (3:97), N-[4-[(3-bromophenyl)amino]-7-[4-(N,N-dimethylamino)butyloxy]-quinazolin-6-yl]acrylamide (98 mg, 32%) as a cream powder, mp (CH2Cl2/Et2O) 112-115° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06602863B1
출처 데이터셋uspto-grants-2003_08
ORD IDord-3cf0751985c642f0bdbf174c484207a6
출처 메모uspto-grants-2003_08