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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 8737생성일: 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/8737

반응식

참여 물질

역할이름HCID투입량
반응물3-(1,2,3,4-Tetrahydro-isoquinolin-5-yl)-pyridin-4-ylamineHCID 21983698—
반응물2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
용매1-MethoxyethanolHCID 3015637—
생성물2-[5-(4-amino-pyridin-3-yl)-3,4-dihydro-1H-isoquinolin-2-yl]-6,7-dimethoxy-3H-quinazolin-4-oneHCID 136011329—

반응 조건

온도95 °C

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-quinazolin-4-one 902. The product was converted to the hydrochloric acid salt, mp. >300° C., [M+H]+=430.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07091200B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-f83e86f633f84f5f9939b049f416c75f
출처 메모uspto-grants-2006_08