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HRID 1290512Erstellt: 25. Oktober 2026

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

https://huagongshe.com/reaction/1290512

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiethyl EtherHCID 3283—
EduktTriethylamineHCID 8471—
Edukt1-(4-Pyridyl)piperazineHCID 70517—
EduktMethyl 2-(4-bromoacetylphenoxy)isobutyrateHCID 18918561—
LösungsmittelAcetonitrileHCID 6342—
Produkt2-[4-[2-[4-(4-Pyridyl)piperazin-1-yl]acetyl]phenoxy]-isobutyric acid, dihydrobromideHCID 131720105—

Reaktionsschritte

The product from step (i) above (2.00 g) in acetonitrile (10 ml) was added dropwise over 15 minutes to a stirred solution of 1-(4-pyridyl)piperazine (1.04 g) and triethylamine (0.89 ml) in acetonitrile (15 ml) and the mixture stirred overnight. The precipitated solid was removed by filtration and the filtrate evaporated. Purification of the residue by flash chromatography on silica, eluting with 0 to 5% v/v methanol/dichloromethane, gave a yellow gum. Trituration of this gum with diethyl ether gave methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutryate, 170 mg, as a white solid: m.p. 88°-90° C.; NMR (d6 DMSO)δ8.15(2H,d), 7.96(2H,d), 6.82(4H,m), 3.92(2H,s), 3.70(3H,s), 3.33(4H,t), 2.63(4H,t), 1.60(6H,s); m/e 398 (M+H)+ ; calculated for C22H27N3O4.0.25H2O: C, 65.8; H, 6.8; N, 10.5. found: C, 65.8 H, 7.1; N, 10.4%.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05750754
Quelldatensatzuspto-grants-1998_05
ORD IDord-3ff2aca72d3145f89c5a3df08b534f28
Quellennotizuspto-grants-1998_05