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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986231Generated: October 30, 2026

2-(5-chloro-2-((3-(4-methylpiperazin-1-yl)propyl)amino)pyrimidin-4-yl)-N-cyclopropylbenzo[b]thiophene-4-carboxamide trihydrochloride → 1-(3-Aminopropyl)-4-methylpiperazine

https://huagongshe.com/reaction/1986231

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(5-chloro-2-((3-(4-methylpiperazin-1-yl)propyl)amino)pyrimidin-4-yl)-N-cyclopropylbenzo[b]thiophene-4-carboxamide trihydrochlorideHCID 68856073—
Reactant2-(2,5-Dichloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid [bis-(4-methoxy-phenyl)-methyl]-amideHCID 86625365—
Product1-(3-Aminopropyl)-4-methylpiperazineHCID 7832865%
Product2-{5-Chloro-2-[3-(4-methyl-piperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid [bis-(4-methoxy-phenyl)-methyl]-amideHCID 86625364—

Reaction Steps

Using the method of Preparation E of 2-{5-chloro-2-[3-(4-methylpiperazin-1-yl)-propylamino]-pyrimidin-4-yl}-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride, the title compound is prepared from 2-(2,5-dichloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid [bis-(4-methoxy-phenyl)-methyl]-amide and 1-(3-aminopropyl)-4-methylpiperazine as a white solid (65% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-52a82456da654ef2acd80d560e4a4314
Source noteuspto-grants-2009_06