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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986265Generated: October 29, 2026

1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazine → 2-[5-Bromo-2-(3-piperazin-1-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride

https://huagongshe.com/reaction/1986265

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazineHCID 17750945—
Reactant2-[5-Chloro-2-(2-piperidin-4-yl-ethylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide di-hydrochlorideHCID 68857850—
Reactant2-(5-Bromo-2-chloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamideHCID 86625343—
Product2-[5-Bromo-2-(3-piperazin-1-yl-propylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochlorideHCID 68858707—

Reaction Steps

Using the synthetic method of 2-[5-chloro-2-(2-piperidin-4-yl-ethylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide di-hydrochloride, the title compound is synthesized from 2-(5-bromo-2-chloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamide and 4-(3-aminopropyl)-piperazine-1-carboxylic acid tert-butyl ester and isolated as a yellow solid (59% yield). ES+(m/z) 515 (79Br) and 517 (81Br) [M(free base)+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-fce01fe175c24992a428795774621b6e
Source noteuspto-grants-2009_06