Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1373335생성일: 2026년 10월 25일
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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 5-Chloro-1,3-benzodioxol-4-amine | HCID 11367253 | — |
| 반응물 | 4-Chloro-5-morpholino-7-(2-pyrrolidin-1-ylethoxy)quinazoline | HCID 22140709 | — |
| 용매 | Isopropanol | HCID 3776 | — |
| 생성물 | N-(5-chloro-1,3-benzodioxol-4-yl)-5-morpholin-4-yl-7-(2-pyrrolidin-1-ylethoxy)quinazolin-4-amine | HCID 11974116 | 9.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07160891B2 |
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| 출처 데이터셋 | uspto-grants-2007_01 |
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| ORD ID | ord-082c60f7772c4840a3033b2a9c607101 |
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| 출처 메모 | uspto-grants-2007_01 |
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