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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1986229Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/1986229

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-tert-Butyloxycarbonyl-4-(3-aminopropyl)piperazineHCID 17750945—
Edukt[4-(Benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochlorideHCID 68855962—
Edukt2-(2,5-Dichloropyrimidin-4-yl)-benzo[b]thiophene-4-carboxylic acid cyclopropylamideHCID 86625351—
Produkt2-[5-Chloro-2-(3-piperazin-1-ylpropylamino)-pyrimidin-4-yl]-benzo[b]thiophene-4-carboxylic acid cyclopropylamide tri-hydrochlorideHCID 68858808—

Reaktionsschritte

Using the method of [4-(benzo[b]thiophen-2-yl)-pyrimidin-2-yl]-[3-(4-methylpiperazin-1-yl)-propyl]-amine tri-hydrochloride, the title compound is synthesized from 2-(2,5-dichloropyrimidin-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 (43% yield). ES+(m/z) 471 (35Cl) and 473 (37Cl) [M+H].

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07547691B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-9ca0ef3201844157afcb75cd78e588a6
Quellennotizuspto-grants-2009_06