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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1167170생성일: 2026년 10월 26일

Triethylamine → 4-[(3-chloro-4-fluorophenyl)amino]-6-cyclopentylmethoxy-7-(2-{4-[(S)-(2-oxo-tetrahydrofuran-5-yl)carbonyl]-piperazin-1-yl}-ethoxy)-quinazoline

https://huagongshe.com/reaction/1167170

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물(2S)-5-oxooxolane-2-carboxylic acidHCID 636468—
반응물O-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
반응물4-[(3-Chloro-4-fluorophenyl)amino]-6-cyclopentylmethoxy-7-[2-(piperazin-1-yl)-ethoxy]-quinazolineHCID 15547168—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물4-[(3-chloro-4-fluorophenyl)amino]-6-cyclopentylmethoxy-7-(2-{4-[(S)-(2-oxo-tetrahydrofuran-5-yl)carbonyl]-piperazin-1-yl}-ethoxy)-quinazolineHCID 15547167—

반응 단계

72 mg of (S)-(+)-5-oxo-tetrahydrofuran-2-carboxylic acid are dissolved in 2.5 ml of N,N-dimethylformamide, combined with 183 mg of (benzotriazol-1-yl)-N,N,N′,N′-tetramethyl-uronium-tetrafluoroborate and stirred for 30 minutes at ambient temperature. This solution is then added to a mixture of 250 mg of 4-[(3-chloro-4-fluorophenyl)amino]-6-cyclopentylmethoxy-7-[2-(piperazin-1-yl)-ethoxy]-quinazoline and 110 μl of triethylamine in 2.5 ml of N,N-dimethylformamide. The reaction mixture is stirred for five hours at ambient temperature. For working up the mixture is poured onto 50 ml of water. A white precipitate is formed, which is suction filtered and washed with water. The crude product is purified by chromatography over an Alox column (activity stage III) with methylene chloride/methanol (98:2) as eluant. The desired product is obtained as a light-coloured solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06617329B2
출처 데이터셋uspto-grants-2003_09
ORD IDord-8ecf5089882d4a92908b45181c6f4ce1
출처 메모uspto-grants-2003_09