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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093652Generated: October 31, 2026

5-(2-benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-[4-(2-chloro-phenoxy)-piperidin-1-yl]-2-oxo-ethyl}-amide → HCID 178523495, compound

https://huagongshe.com/reaction/1093652

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-(2-benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-[4-(2-chloro-phenoxy)-piperidin-1-yl]-2-oxo-ethyl}-amideHCID 178523494—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 178523495HCID 17852349583%

Reaction Steps

To a solution of 5-(2-benzyloxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-[4-(2-chloro-phenoxy)-piperidin-1-yl]-2-oxo-ethyl}-amide (0.075 g, 0.00014 mole), in methanol (50 mL) was added 10% Pd/C (0.015 g) and the resulting mixture was stirred under an atmosphere of hydrogen for 1.5 hours. The mixture was then filtered through celite, the celite was washed with methanol and the organic layers were concentrated under reduced pressure. The resulting residue was recrystallized from a mixture of ethyl acetate and methanol to afford 0.052 g (83%) of 5-(2-hydroxy-phenyl)-1H-pyrazole-3-carboxylic acid {2-[4-(2-chloro-phenoxy)-piperidin-1-yl]-2-oxo-ethyl}-amide. LCMS: 455.16 (M+1)+, 90.34%, 1H NMR (DMSO-d6): δ 13.2 (s, 1H), 10.2 (s, 1H), 8.0 (s, 1H), 7.64 (m, 1H), 7.42 (m, 1H), 7.24 (m, 2H), 7.18 (m, 1H), 7.06 (s, 1H), 6.96 (m, 2H), 6.84 (t, 1H), 4.7 (m, 1H), 4.2 (d, 2H), 3.61 (m, 2H), 3.4 (m, 2H), 1.9 (m, 2H), 1.6 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-949bed17e1e44aab94461b39633fb21a
Source noteuspto-grants-2012_03