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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093673Generated: October 30, 2026

HCID 57874431, compound → HCID 57874485, compound

https://huagongshe.com/reaction/1093673

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 57874431HCID 57874431—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 57874485HCID 5787448530.6%

Reaction Steps

To a solution of N-biphenyl-4-yl-3-[4-(2-nitro-phenoxy)-piperidin-1-yl]-3-oxo-propionamide (0.09 g, 0.00019 mole) in methanol (10 mL) was added 10% Pd/C (0.015 g) and the resulting mixture was stirred under an atmosphere of hydrogen for 30 minutes. 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 hexane and chloroform to afford 0.025 g (29%) of 3-[4-(2-amino-phenoxy)-piperidin-1-yl]-N-biphenyl-4-yl-3-oxo-propionamide. LC-MS purity: 430.21 (M+1)+, 90.7%, 1H NMR (DMSO-d6): δ 7.7 (m, 6H), 7.4 (m, 2H), 7.3 (m, 1H), 6.8 (m, 1H), 6.6 (m, 2H), 6.5 (m, 1H), 4.6 (bs, 2H), 4.5 (bs, 1H), 3.8 (m, 2H), 3.5 (m, 4H), 2.0 (m, 2H), 1.8 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08129376B2
Source datasetuspto-grants-2012_03
ORD IDord-3ef06eb8a4b84800a24efaefc0fb5cc5
Source noteuspto-grants-2012_03