Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266738Generated: October 26, 2026

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

https://huagongshe.com/reaction/266738

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
Reactant1,4-DioxaneHCID 31275—
ReactantMethyl 2-[4-[2-[4-(4-pyridyl)piperazin-1-yl]acetyl]phenoxy]isobutyrateHCID 18918633—
SolventWaterHCID 962—
Product2-[4-[2-[4-(4-Pyridyl)piperazin-1-yl]acetyl]phenoxy]-isobutyric acid, dihydrobromideHCID 131720105—

Reaction Conditions

Temperature95 °C

Reaction Steps

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, 3.6; H, 5.3; N,

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652242
Source datasetuspto-grants-1997_07
ORD IDord-cc776742887848d99a5db5a1d1955b88
Source noteuspto-grants-1997_07