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HRID 2264351Erstellt: 25. Oktober 2026

2,9-Dimethyl-1,10-phenanthroline → 4-(6-Amino-pyridin-3-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/2264351

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,9-Dimethyl-1,10-phenanthrolineHCID 65237—
Edukt2-Pyridinamine, 5-iodo-HCID 88579—
EduktMagnesiumHCID 5462224—
Edukttert-Butyl 4-sulfanylpiperidine-1-carboxylateHCID 21906090—
EduktSodium t-butoxideHCID 23676156—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTolueneHCID 1140—
Produkt4-(6-Amino-pyridin-3-ylsulfanyl)-piperidine-1-carboxylic acid tert-butyl esterHCID 6742732081,4%

Reaktionsbedingungen

Temperatur110 °C

Reaktionsschritte

Add dry toluene (6.06 mL) to a mixture of 2,9-dimethyl-1,10-phenanthroline (76.52 mg), copper(I) iodide (69.27 mg), sodium tert-butoxide (475.59 mg), 4-mercapto-piperidine-1-carboxylic acid tert-butyl ester (583.5 mg), magnesium (49.10 mg) and 2-amino-5-iodopyridine (550 mg). Bubble nitrogen into the mixture with ultrasound and stir the suspension at 110° C. in a sealed tube for 24 h. Cool and filter through celite. Wash with toluene and remove the solvent under vacuum. Add hexane/EA (1/1) and filter through a celite/silica gel pad, washing twice with hexane/EA (1/1) and then EA. Remove the solvent under vacuum. Purify by silica gel column chromatography eluting with hexane/EA (50-75%) to afford 630 mg of the title compound. MS (ES+): m/z=310 (M+H)+

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07855211B2
Quelldatensatzuspto-grants-2010_12
ORD IDord-bee74f59518041d09dfddf5b94f00686
Quellennotizuspto-grants-2010_12