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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 132289Erstellt: 25. Oktober 2026

Sodium Bicarbonate → Methyl 3-{2-[(acetyloxy)methyl]-4-[(tert-butoxycarbonyl)amino]-3-methylphenyl}-2-{[(benzyloxy)carbonyl]amino}prop-2-enoate

https://huagongshe.com/reaction/132289

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
EduktZ-Dehydro-Ala-OMeHCID 3525700—
Edukt3-(Tert-butoxycarbonylamino)-6-iodo-2-methylbenzyl acetateHCID 53414707—
Katalysatorpalladium(II) acetateHCID 167845—
KatalysatorTetrabutylammonium chloride hydrateHCID 16212273—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktMethyl 3-{2-[(acetyloxy)methyl]-4-[(tert-butoxycarbonyl)amino]-3-methylphenyl}-2-{[(benzyloxy)carbonyl]amino}prop-2-enoateHCID 5341513869%

Reaktionsschritte

Palladium (II) acetate (105 mg, 0.43 mmol) was added to a mixture of acetic acid 3-tert-butoxycarbonylamino-6-iodo-2-methyl-benzyl ester (2.89 g, 7.1 mmol), Z-dehydroalanine methyl ester (2.20 g, 9.4 mmol), tetrabutylammonium chloride hydrate (2.70 g, 9.7 mmol), and sodium bicarbonate (1.80 g, 21.4 mmol) in THF (100 mL). Reaction was heated at reflux for 3.75 hours. Mixture was cooled to room temperature then filtered through a plug of silica gel eluting 70% ethyl acetate-hexanes (500 mL). Filtrate was concentrated in vacuo. Silica gel chromatography afforded the title compound as a yellow solid in 69% yield. 1H NMR (300 MHz, CDCl3): δ=7.79 (d, J=8.4, 1H), 7.42 (s, 1H), 7.27 (m, 6H), 6.30 (s, 1H), 5.11 (s, 2H), 5.02 (s, 2H), 3.81 (s, 3H), 2.21 (s, 3H), 2.02 (s, 3H), 1.51 (s, 9H). MS m/e (M−H)−=511.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07384931B2
Quelldatensatzuspto-grants-2008_06
ORD IDord-439f2396daaf45e8a85daf34b08fefa2
Quellennotizuspto-grants-2008_06