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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 551587Erstellt: 25. Oktober 2026

1,2-Dichloroethane → (4-Isopropyl-piperazin-1-yl)-[6-(2-piperidin-1-yl-ethylamino)-pyridin-3-yl]-methanone

https://huagongshe.com/reaction/551587

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
Edukt4-MethylmorpholineHCID 7972—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1-IsopropylpiperazineHCID 78013—
Edukt6-Chloronicotinic acidHCID 79222—
Edukt(6-Chloro-pyridin-3-yl)-(4-isopropyl-piperazin-1-yl)-methanoneHCID 43420904—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelSodium HydroxideHCID 14798—
ProduktAmmoniaHCID 2222%
Produkt(4-Isopropyl-piperazin-1-yl)-[6-(2-piperidin-1-yl-ethylamino)-pyridin-3-yl]-methanoneHCID 1171021256%

Reaktionsschritte

(6-Chloro-pyridin-3-yl)-(4-isopropyl-piperazin-1-yl)-methanone. To a solution of 6-chloronicotinic acid (0.985 g, 6.25 mmol) and 1-isopropyl-piperazine (1.50 g, 7.50 mmol) in DCM (100 mL) was added HOBt (1.20 g, 9.40 mmol), EDC (1.80 g, 9.40 mmol), and N-methyl morpholine (3.4 mL, 31.3 mmol). After 18 h the reaction was diluted with 1 N NaOH (50 mL) and extracted with DCM (3×50 mL). The organic extracts were combined, dried (Na2SO4), and concentrated. Chromatography of the residue (SiO2: 2-4% 2 M NH3 in MeOH/DCM) gave the title compound as a solid (0.934 g, 56%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07947718B2
Quelldatensatzuspto-grants-2011_05
ORD IDord-f19ecca019454a139282c3ef390b44e3
Quellennotizuspto-grants-2011_05