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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 50773Erstellt: 26. Oktober 2026

Carbon Dioxide → 4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acid

https://huagongshe.com/reaction/50773

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktCarbon DioxideHCID 280—
EduktDiethyl EtherHCID 3283—
Edukt4-(Boc-amino)pyridineHCID 9990210—
EduktButyllithiumHCID 178418339—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-{[(Tert-butoxy)carbonyl]amino}pyridine-3-carboxylic acidHCID 2217262354%

Reaktionsbedingungen

Temperatur-78 °C

Reaktionsschritte

n-Butyl lithium (2.18 M, 24 mL, 52.51 mmol) is added slowly to a solution of 4-(N-t-butoxycarbonylamino)-pyridine (4.08 g, 21 mmol) in THF (50 mL, stirred under N2 at −78° C. The solution is allowed to warm to 0° C., stirred for 3 h, then cooled again to −78° C. and poured into ether (100 mL) containing dry ice. The solution is warmed to room temperature with constant stirring. Water is added and the mixture is neutralized with acetic acid. The resulting solid is collected by vacuum filtration and dried in a vacuum oven to give 4-(N-t-butoxycarbonylamino)nicotinic acid (2.72 g, 54%) as a brown solid. 1H NMR (DMSO) δ 11.75 (1H, brs), 8.95 (1H, s), 8.50 (1H, d, J=6.0 Hz) 8.20 (1H, d, J=6.0 Hz), 1.49 (9H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06713484B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-b4e7f44004264174a2fd5c2c996aaf75
Quellennotizuspto-grants-2004_03