Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2238398Erstellt: 25. Oktober 2026

tert-Butanol → Methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoate

https://huagongshe.com/reaction/2238398

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukttert-ButanolHCID 6386—
EduktTriethylamineHCID 8471—
EduktP,P-Diphenylphosphinic azideHCID 199401—
EduktSodium BicarbonateHCID 516892—
Edukt6-(Methoxycarbonyl)naphthalene-2-carboxylic acidHCID 3380217—
ProduktMethyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoateHCID 4454953278%

Reaktionsschritte

A suspension of 6-(methoxycarbonyl)-2-naphthoic acid [J. Med. Chem., 2004, 47, 303-324] (146) (1.21 g, 5.26 mmol) in dry t-BuOH (20 mL) containing powdered molecular sieves (1 g) was treated with Et3N (0.88 mL, 6.31 mmol) and stud under N2 at room temperature for 30 min. DPPA (1.25 mL, 5.80 mmol) was added and the mixture was sired at reflux for 7 h, then cooled and poured into dilute aqueous NaHCO3. The resting solid was purified by chromatography on silica gel, eluting with CH2Cl2, followed by trituration with iPr2O and recrystallization from EtOAc to give methyl 6-[(tert-butoxycarbonyl)amino]-2-naphthoate (147) (1.24 g, 78%) as a white solid: mp 178-180° C.; 1H NMR [(CD3)2SO] δ 9.76 (s, 1H), 8.51 (s, 1H), 8.19 (s, 1H), 8.02 (d, J=9.0 Hz, 1H), 7.90 (dd, J=8.6, 1.6 Hz, 1H), 7.86 (d, J=8.7 Hz, 1H), 7.59 (dd, J=8.9, 2.1 Hz, 1H), 3.89 (s, 3H), 1.52 (s, 9H). Anal. (C17H19NO4) C, H, N.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07718688B2
Quelldatensatzuspto-grants-2010_05
ORD IDord-bd1c72b315d944a6b7df28551dc9fefd
Quellennotizuspto-grants-2010_05