Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 471772Erstellt: 25. Oktober 2026

1-Azido-2-methoxyethane → 2-Amino-6-(1-(2-methoxyethyl)-1H-1,2,3-triazol-4-yl)benzonitrile

https://huagongshe.com/reaction/471772

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Azido-2-methoxyethaneHCID 12858399—
EduktSodium AscorbateHCID 23667548—
Edukt2-Amino-6-ethynylbenzonitrileHCID 86657482—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelWaterHCID 962—
Lösungsmittel2-Methylpropan-2-ol--water (1/1)HCID 71401949—
Produkt2-Amino-6-(1-(2-methoxyethyl)-1H-1,2,3-triazol-4-yl)benzonitrileHCID 6740006888%

Reaktionsschritte

To a solution of 1-bromo-2-methoxyethane (5.00 g, 35.97 mmol) in DMF (25 mL), was added sodium azide (3 equiv.) and the mixture was heated at 50° C. for 48 hours. The reaction mixture was diluted with water (75 mL) and extracted with diethyl ether. The organic extract was dried over MgSO4 and concentrated to furnish 1-azido-2-methoxyethane as a yellow liquid. This azide (200 mg, 1.94 mmol) was added to a solution of 2-Amino-6-ethynylbenzonitrile (250 mg, 1.76 mmol) (Example 267c) in H2O/tert-BuOH=1:2 (15 mL) and the solution was treated consecutively with sodium ascorbate (0.264 mmol) and CuSO4 (0.035 mmol). The reaction mixture was stirred at room temperature for 48 hours, diluted with water and extracted with ethyl acetate. The organic extract was dried over MgSO4 and purified over silica gel (ethyl acetate/hexane 6:4) to furnish the title compound as a white solid in 88% yield. 1H NMR (400 MHz, DMSO-d6) δ 3.26 (s, 3H), 3.78 (t, J=5.2 Hz, 2H), 4.23 (t, J=5.2 Hz, 2H), 6.13 (br s, 2H), 6.80 (dd, J=1.2, 8.4 Hz, 1H), 7.09 (dd, J=1.2, 7.6 Hz, 1H), 7.36 (t, J=8.4 Hz, 1H), 8.52 (s, 1H). MS 244 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08633186B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-adaf97ac45984af09f1cdb706b1a25b0
Quellennotizuspto-grants-2014_01