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HRID 79209Erstellt: 25. Oktober 2026

Triethylamine → tert-Butyl 4-(2-chloronicotinoyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/79209

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukttert-Butyl piperazine-1-carboxylateHCID 143452—
Edukt6-Chloronicotinoyl ChlorideHCID 2782165—
EduktDichloromethane methanolHCID 21226129—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-Butyl 4-(2-chloronicotinoyl)piperazine-1-carboxylateHCID 432161989%

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

To a stirred ice-cooled solution of tert-butyl 1-piperazinecarboxylate (2.2 g, 12 mmol), triethylamine (3.2 mL, 23 mmol), and 4-dimethylaminopyridine (0.014 g, 0.11 mmol) in DCM (15 mL) was added 6-chloropyridine-3-carbonyl chloride (2.0 g, 11 mmol) in one portion. The resulting mixture was stirred at 0° C. and gradually warmed up to ambient temperature for 20 h. Upon workup, the mixture was subjected to combi-flash column chromatography (methanol/DCM) to give compound 351 (3.3 g, 89% yield) as a white solid. 1H NMR (400 MHz, CDCl3) δ ppm 8.46 (1 H, d, J=2.0 Hz), 7.74 (1 H, dd, J=8.2, 2.3 Hz), 7.42 (1 H, dd, J=8.2, 0.8 Hz), 3.20-4.02 (8 H, m), 1.48 (9 H, s). LCMS-ESI (POS), M/Z, M+1: Found 326.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08841312B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-af2914b2e197410da17757f6a76e2c5a
Quellennotizuspto-grants-2014_09