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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 243625Erstellt: 26. Oktober 2026

octanedioic acid [4-(3-Nitro-phenyl)-thiazol-2-yl]-amide methyl ester → octanedioic acid [4-(3-Amino-phenyl)-thiazol-2-yl]-amide methyl ester

https://huagongshe.com/reaction/243625

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktoctanedioic acid [4-(3-Nitro-phenyl)-thiazol-2-yl]-amide methyl esterHCID 44550802—
KatalysatorPalladiumHCID 23938—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelEthanolHCID 702—
Produktoctanedioic acid [4-(3-Amino-phenyl)-thiazol-2-yl]-amide methyl esterHCID 4455093072,4%

Reaktionsschritte

A suspension of compound 14 (0.391 g, 1 mmol) and Pd/C (10 wt. %, 50 mg) in EtOH and AcOH (20 ml+1 ml) was reacted under hydrogen atmosphere at 50° C. for 2 hours. The catalyst was removed by filtration through a pad of Celite. After removal of the solvent in vacuo, the crude material was dissolved in EtOAc and washed with NaHCO3 solution and brine and dried over Na2SO4. The solvent was removed by rotary evaporation. The crude solid was purified by flash chromatography (EtOAc/hexane, 2:1) to give compound 20 (0.261 g, 72.4%). 1H NMR (300 MHz, CDCl3) δ 11.2 (1H, s), 7.22 (1H, s), 7.20 (1H, s), 7.16 (1H, brs), 7.10 (1H, s), 6.70-6.66 (1H, m), 3.69 (3H, s), 2.28 (2H, t, J=7.4 Hz), 2.06 (2H, dd, J=7.3, 4.7 Hz), 1.61-1.45 (4H, m), 1.22-1.08 (4H, m). 13C NMR (75 MHz, CDCl3) δ 174.6, 171.8, 159.6, 150.1, 147.3, 135.7, 130.2, 116.9, 115.3, 113.0, 108.1, 51.9, 36.1, 34.3, 29.07, 29.01, 25.09, 25.00, 21.4.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08653278B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-7d7cc4d73072448797ac305437d34c6e
Quellennotizuspto-grants-2014_02