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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1414283생성일: 2026년 10월 27일

1,2-Ethanediamine, N1,N1-bis(1-methylethyl)- → N-(2-diisopropylaminoethyl)-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarboxamide

https://huagongshe.com/reaction/1414283

반응식

참여 물질

역할이름HCID투입량
반응물1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
반응물TriethylamineHCID 8471—
반응물6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarbonyl chlorideHCID 21486964—
용매ChloroformHCID 6212—
생성물N-(2-diisopropylaminoethyl)-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarboxamideHCID 21487010—

반응 단계

4.0 Parts of 2-diisopropylaminoethylamine in 75 parts of chloroform is added portionwise, at room temperature, to a mixture of 8.0 parts of 6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarbonyl chloride and 15 parts of triethylamine in 225 parts of chloroform. After the addition is complete, the mixture is stirred for 3 to 4 hours, allowed to stand overnight, and then washed with water. The chloroform layer is separated, dried over anhydrous calcium sulfate and concentrated under reduced pressure. The solid material obtained in this manner is crystallized from ether to give N-(2-diisopropylaminoethyl)-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarboxamide, melting at about 114°-115°C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04001244
출처 데이터셋uspto-grants-1977_01
ORD IDord-3668809edd3f4ec5a21be884fe9ad38e
출처 메모uspto-grants-1977_01