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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 130755Erstellt: 26. Oktober 2026

1-Cyclopentylpiperazine → HCID 59730338, Verbindung

https://huagongshe.com/reaction/130755

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-CyclopentylpiperazineHCID 806421—
EduktSodium borohydrideHCID 4311764—
Edukt6-(4-Formylphenoxy)pyridine-3-carboxamideHCID 56851422—
LösungsmittelMethanolHCID 887—
ProduktHCID 59730338HCID 5973033836,2%

Reaktionsschritte

Combine 6-(4-formyl-phenoxy)-nicotinamide (compound of example 332, step 1) (0.303 g, 1.25 mmol) and 1-cyclopentyl piperazine (0.198 g, 1.28 mmol) in methanol (11 mL) and stir. After 15.5 h, add sodium borohydride (0.109 g, 2.88 mmol), and stir at ambient temperature. After 1 h, concentrate the reaction mixture and purify by silica gel chromatography (ethyl acetate→4:1 ethyl acetate:methanol) to provide 0.172 g (36%) of the title compound as an off white solid: high resolution mass spectrum (electrospray): m/z calc for C22H29N4O2 381.2291, found 381.2306; 1H NMR (DMSO-d6): 8.66 (d, 1H, J=2.4 Hz), 8.30 (dd, 1H, J=2.9, 8.8 Hz), 7.48-7.43 (m, 2H), 7.18-7.13 (m, 2H), 7.04 (d, 1H, J=7.8 Hz), 3.61 (s, 2H), 3.00-2.25 (m, 9H), 2.01-1.88 (m, 2H), 1.82-1.69 (m, 2H), 1.69-1.56 (m, 2H), 1.53-1.38 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07381719B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-500fdcd8ff9848fe94c4841e5bd5c97a
Quellennotizuspto-grants-2008_06