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HRID 323030Erstellt: 24. Oktober 2026

Triethylamine → HCID 21184722, Verbindung

https://huagongshe.com/de/reaction/323030

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktDiphenylphosphoryl azideHCID 123414—
Edukt3-Methoxythiophene-2-carboxylic acidHCID 1483475—
Edukt2-Amino-5-NitrophenolHCID 4984721—
LösungsmittelTolueneHCID 1140—
ProduktHCID 21184722HCID 2118472248%

Reaktionsbedingungen

Temperatur70 °C

Reaktionsschritte

To a solution of 3-methoxy-2-thiophene carboxylic acid (example 11a, 200 mg, 1.27 mmol) in toluene, (PhO)2PON3 (0.33 mL) and triethylamine (1. 1 equiv., 0.25 mL) were added. The reaction mixture was stirred at 70° C. for 2 hours and cooled down to room temperature then 2-amino-5-nitrophenol was added. The reaction mixture was stirred at 70° C. overnight. The reaction mixture was partitioned between 5% citric acid and ethyl acetate. The organic layer was separated and the aqueous layer was extracted three times with ethyl acetate. The organic extracts were combined, dried over MgSO4, filtered and concentrated under reduced pressure. Chromatography of the resulting solid on silica gel (hexane:ethyl acetate; 1:1) gave the product (190 mg, 48%). 1H NMR (CD3OD/CDCl3): d 8.38 (d, 1H, J=5.0 Hz), 7.85 (dd, 1H, J=5.0 Hz and J=1.25 Hz), 7.76 (d, 1H, J=2.5 Hz), 6.9 (s, 2H), 3.95 (s, 3H); El-MS m/z 309 (M+H)+; Anal. (C12H11N3O5S) C, H, N.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06211373B1
Quelldatensatzuspto-grants-2001_04
ORD IDord-c406b686b9b4498daa885b644e06ad84
Quellennotizuspto-grants-2001_04