Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2183721생성일: 2026년 10월 24일
3-(1,2,3,4-Tetrahydro-isoquinolin-5-yl)-pyridin-4-ylamine → 2-[5-(4-amino-pyridin-3-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-6,7-dimethoxy-3H-quinazolin-4-one
https://huagongshe.com/ko/reaction/2183721
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 3-(1,2,3,4-Tetrahydro-isoquinolin-5-yl)-pyridin-4-ylamine | HCID 21983698 | — |
| 반응물 | 2-Chloro-6,7-dimethoxy-3H-quinazolin-4-one | HCID 135456664 | — |
| 용매 | 1-Methoxyethanol | HCID 3015637 | — |
| 생성물 | 2-[5-(4-amino-pyridin-3-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-6,7-dimethoxy-3H-quinazolin-4-one | HCID 136011329 | — |
반응 단계
A mixture of 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b (0.076 g, 0.31 mmol) and 3-(1,2,3,4-tetrahydro-isoquinolin-5-yl)-pyridin-4-ylamine (0.075 g, 0.33 mmol) in methoxyethanol (5 mL) was heated to 95° C. with stirring for 18 h the volatiles were evaporated and the residue was purified by flash column eluting with 2% methanol in dichloromethane containing 0.2% of ammonium hydroxide to yield 2-[5-(4-amino-pyridin-3-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-6,7-dimethoxy-3H-quinazol-4-one 902. The product was converted to the hydrochloric acid salt, mp. >300° C., [M+H]+=430.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06900220B2 |
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| 출처 데이터셋 | uspto-grants-2005_05 |
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| ORD ID | ord-0771b12e627c4dc6a9f8e91bd3f3a565 |
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| 출처 메모 | uspto-grants-2005_05 |
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