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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1414283Generated: October 25, 2026

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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-Ethanediamine, N1,N1-bis(1-methylethyl)-HCID 8459—
ReactantTriethylamineHCID 8471—
Reactant6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarbonyl chlorideHCID 21486964—
SolventChloroformHCID 6212—
ProductN-(2-diisopropylaminoethyl)-6,7-dimethoxy-1-(3,4-dimethoxyphenyl)-3,4-dihydro-2(1H)-isoquinolinecarboxamideHCID 21487010—

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04001244
Source datasetuspto-grants-1977_01
ORD IDord-3668809edd3f4ec5a21be884fe9ad38e
Source noteuspto-grants-1977_01