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HRID 272452Erstellt: 24. Oktober 2026

Tert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylate → tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate

https://huagongshe.com/de/reaction/272452

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-butyl 4-(6-nitropyridin-3-yl)piperazine-1-carboxylateHCID 11243758—
EduktHCID 178418361HCID 178418361—
KatalysatorNickelHCID 935—
LösungsmittelMethanolHCID 887—
Produkttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 1173752583,4%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

4-(6-Nitro-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (83 g, 0.269 mol) in methanol (1.3 L) plus Raney Nickel (15 g, 50% slurry in water) were placed in a Parr shaker and hydrogenated at 50 psi of hydrogen for 5 h. The reaction mixture was filtered through a pad of celite and concentrated to a brown solid. This material was triturated with diethyl ether (120 mL) for 4 h. Heptane was added and the mixture was cooled to 0° C. for 45 min. The solid was collected by filtration and dried to afford the product 4-(6-amino-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester as a tan solid (62.46 g, 83%). mp 130-132° C. MS (ESI); M++1: Calc'd, 279.2. Found 279. Anal. Calc'd for C14H22N4O3: C, 60.41; H, 7.97; N, 20.13. Found; C, 60.45; H, 7.60; N, 19.87.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07456168B2
Quelldatensatzuspto-grants-2008_11
ORD IDord-4ebb6625dc78414182e168a059fb514e
Quellennotizuspto-grants-2008_11