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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1986236Generated: October 25, 2026

1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazine → {2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophen-6-yl}-morpholin-4-ylmethanone tri-hydrochloride

https://huagongshe.com/reaction/1986236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazineHCID 17750945—
Reactant2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochlorideHCID 68858808—
Reactant[2-(2,5-Dichloropyrimidin-4-yl)-benzo[b]thiophen-6-yl]-morpholin-4-yl-methanoneHCID 86625368—
Product{2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophen-6-yl}-morpholin-4-ylmethanone tri-hydrochlorideHCID 68854855—

Reaction Steps

Using the method of 2-[5-chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochloride, the title compound is synthesized from [2-(2,5-dichloropyrimidin-4-yl)-benzo[b]thiophen-6-yl]-morpholin-4-yl-methanone and 4-(3-aminopropyl)-piperazine-1-carboxylic acid tert-butyl ester and isolated as a yellow solid. ES+(m/z) 501 (35Cl) and 503 (37Cl) [M+H].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07547691B2
Source datasetuspto-grants-2009_06
ORD IDord-fc216141a5134b5ba6052f6eb1e5cce7
Source noteuspto-grants-2009_06