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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373335생성일: 2026년 10월 26일

5-Chloro-1,3-benzodioxol-4-amine → N-(5-chloro-1,3-benzodioxol-4-yl)-5-morpholin-4-yl-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine

https://huagongshe.com/reaction/1373335

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참여 물질

역할이름HCID투입량
반응물5-Chloro-1,3-benzodioxol-4-amineHCID 11367253—
반응물4-Chloro-5-morpholino-7-(2-pyrrolidin-1-ylethoxy)quinazolineHCID 22140709—
용매IsopropanolHCID 3776—
생성물N-(5-chloro-1,3-benzodioxol-4-yl)-5-morpholin-4-yl-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amineHCID 119741169.4%

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온도80 °C

반응 단계

A mixture of 4-chloro-5-morpholino-7-(2-pyrrolidin-1-ylethoxy)quinazoline (0.27 g), 6-chloro-2,3-methylenedioxyaniline (0.14 g) and isopropanol (4 ml) was stirred and heated to 80° C. for 1 hour. The mixture was evaporated and the residue was dissolved in a 49:1 mixture of methylene chloride and a saturated methanolic ammonia solution. The mixture was filtered and the filtrate was poured onto a column of silica and eluted with a 97:3 mixture of methylene chloride and a saturated methanolic ammonia solution. The material so obtained was triturated under diethyl ether. The resultant solid was isolated, washed with diethyl ether and dried under vacuum. There was thus obtained the title compound (0.035 g); NMR Spectrum: (CDCl3) 1.85 (br s, 4H), 2.65 (br s, 4H), 3.0 (m, 2H), 3.08 (m, 2H), 3.18 (d, 2H), 3.82 (m, 2H), 4.05 (m, 2H), 4.25 (m, 2H), 6.05 (s, 2), 6.75 (d, 1H), 6.95–7.1 (m, 3H), 8.52 (s, 1H); Mass Spectrum: M+H+ 498 and 500.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07160891B2
출처 데이터셋uspto-grants-2007_01
ORD IDord-082c60f7772c4840a3033b2a9c607101
출처 메모uspto-grants-2007_01