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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2183704생성일: 2026년 10월 25일

Triethylamine → 6,7-dimethoxy-2-[5-(4-methyl-piperazine-1-sulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]-3H-quinazolin-4-one

https://huagongshe.com/reaction/2183704

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물5-(4-Methyl-piperazine-1-sulfonyl)-1,2,3,4-tetrahydro-isoquinolineHCID 21983653—
반응물2-Chloro-6,7-dimethoxy-3H-quinazolin-4-oneHCID 135456664—
용매Dimethyl SulfoxideHCID 679—
용매WaterHCID 962—
생성물6,7-dimethoxy-2-[5-(4-methyl-piperazine-1-sulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]-3H-quinazolin-4-oneHCID 13601132837.2%

반응 조건

온도80 °C

반응 단계

A mixture of 2-chloro-6,7-dimethoxy-3H-quinazolin-4-one 1b, (0.77 g, 3.23 mmol), 5-(4-methyl-piperazine-1-sulfonyl)-1,2,3,4-tetrahydro-isoquinoline 11a (1.25 g, 3.41 mmol) and triethylamine (0.75 g, 1.04 mL, 7.46 mmol) in DMSO (15 mL) was heated at 80° C. with stirring for 18 h. After cooling to room temperature the reaction was diluted with water. The precipitated white product was collected by filtration, washed with water, and dried to give 0.6 g of 6,7-dimethoxy-2-[5-(4-methyl-piperazine-1-sulfonyl)-3,4-dihydro-1H-isoquinolin-2-yl]-3H-quinazolin-4-one 401, mp. 230-237° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06900220B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-1a02fd9b6cfd4f12bf4e4557b49327e7
출처 메모uspto-grants-2005_05