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HRID 1290511Erstellt: 25. Oktober 2026

Hydrogen Bromide → 2-[4-[2-[4-(4-Pyridyl)piperazin-1-yl]acetyl]phenoxy]-isobutyric acid, dihydrobromide

https://huagongshe.com/reaction/1290511

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrogen BromideHCID 260—
Edukt1,4-DioxaneHCID 31275—
EduktMethyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrateHCID 18918633—
LösungsmittelWaterHCID 962—
Produkt2-[4-[2-[4-(4-Pyridyl)piperazin-1-yl]acetyl]phenoxy]-isobutyric acid, dihydrobromideHCID 131720105—

Reaktionsbedingungen

Temperatur95 °C

Reaktionsschritte

A mixture of methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]-isobutyrate (50 mg) 48% w/v hydrobromic acid (0.74 ml), dioxane (1 ml) and water (3 ml) was heated at 95° C. for 4 hours. The solution was cooled, diluted with water and freeze-dried to give the title compound, 40 mg, as a pale yellow solid: m.p. 163°-167° C.; NMR (D2O) δ8.40(2H,d), 8.16(2H,d), 7.40(2H,d), 7.21(2H,d), 5.21(2H,s), 4.32(4H,b), 3.89(4H,bt), 1.86(6H,s), m/e 384 (M+H)+ ; calculated for C21H25 N3.2HBr.2H2O: C, 43.3; H, 5.3; N, 7.2. found: C, 43.6; H, 5.3; N, 7.3%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05750754
Quelldatensatzuspto-grants-1998_05
ORD IDord-f0d67188c93a43cfaec9c87846c85cc4
Quellennotizuspto-grants-1998_05