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HRID 80641Erstellt: 23. Oktober 2026

Azidomethyl 2,2-dimethylpropanoate → (4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalate

https://huagongshe.com/de/reaction/80641

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAzidomethyl 2,2-dimethylpropanoateHCID 11521126—
EduktWater butanolHCID 22253497—
EduktSodium AscorbateHCID 23667548—
Edukt5-(Prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridineHCID 57708431—
KatalysatorCopper SulfateHCID 24462—
LösungsmittelWaterHCID 962—
Produkt(4-((6-(1H-Tetrazol-1-yl)pyridin-3-yloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl pivalateHCID 57708433—

Reaktionsschritte

To a solution of azidomethyl pivalate (4.26 g, 27.1 mmol) in 1:1 text -butanol water (90 mL total) was added 5-(prop-2-ynyloxy)-2-(1H-tetrazol-1-yl)pyridine (5.45 g, 27.1 mmol), sodium ascorbate (1.4 mL of a 1M solution in water) and copper sulfate (1.4 mL of a 1M solution in water). The solution was stirred at room temperature for 72 hours. Water was added and the suspension was extracted with ethyl acetate. The organic layer was separated, dried over sodium sulfate, filtered and concentrated in vacuo to afford the expected product which was used in the next step without further purification. 1H NMR (DMSO-d6): δ 10.07 (1H, s), 8.43-8.41 (2H, m), 8.00 (1H, d, J=8.8 Hz), 7.88 (1H, dd, J=3.2, 8.8 Hz), 6.32 (2H, s), 5.38 (2H, s), 1.08 (9H, s).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08846675B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-6cb9a023f229469fa1e8821c6da6f32f
Quellennotizuspto-grants-2014_09