Reaktion #2312

ord-76266dbb7ecd40f78d7b97f8f4934f98

Reaktionsgleichung

COC(=O)C(C)(C)Oc1ccc(C(=O)CN2CCN(c3ccncc3)CC2)cc1
methyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]-acetyl]phenoxy]isobutyrate
Br
hydrobromic acid
C1COCCO1
dioxane
Br.Br.CC(C)(Oc1ccc(C(=O)CN2CCNCC2c2ccncc2)cc1)C(=O)O
title compound
Br.Br.CC(C)(Oc1ccc(C(=O)CN2CCNCC2c2ccncc2)cc1)C(=O)O
2-[4-[2-[2-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]-isobutyric acid, dihydrobromide

Lösungsmittel

Reaktionsbedingungen

Temperatur
95°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    TemperaturThe solution was cooled
  2. 2
    Sonstigefreeze-dried

Vorschrift

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) δ 8.40 (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 C21H25N3.2HBr.2H2O: C, 43.3; H, 5.3; N, 7.2. found: C, 43.6; H, 5.3; N, 7.3%.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05728701uspto-grants-1998_03