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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2266256Generated: November 3, 2026

HCID 68691509, compound → HCID 57918939, compound

https://huagongshe.com/reaction/2266256

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 68691509HCID 68691509—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
ProductHCID 57918939HCID 5791893936%

Reaction Steps

To a solution of (S)-tert-butyl 3-(4-acetamido-1-(6-fluoro-3′-methylbiphenyl-3-yl)but-1-enyl)piperidine-1-carboxylate (110 mg, 0.85 mmol) in anhydrous MeOH (3 mL) was added anhydrous Pd(OH)2 (20 mg). The reaction mixture was stirred overnight under a hydrogen atmosphere (monitored by LC-MS) and filtered through a plug of silica. The filtrate was concentrated in vacuo to afford a mixture with two isomers. Purification by preparative HPLC gave (S)-tert-butyl 3-((R)-4-acetamido-1-(6-fluoro-3′-methylbiphenyl-3-yl)butyl)piperidine-1-carboxylate (40 mg, 36% yield). 1H NMR (400 MHz, MeOH):7.31-7.37 (m, 2 H), 7.20 (d, 2 H), 7.13 (d, 2 H), 6.97-7.01 (m, 3 H), 3.95-4.18 (m, 1 H), 3.80-3.92 (m, 1 H), 3.03 (m, 2 H), 2.61-2.72 (m, 1 H), 2.42-2.52 (m, 1 H), 2.38 (d, 3 H), 1.90 (s, 3 H), 1.78 (m, 1 H), 1.42-1.65 (m, 4 H), 1.43 (s, 9 H), 1.15-1.31 (m, 3 H), 1.03 (m, 1 H). MS (E/Z): 483 (M+H+)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07858624B2
Source datasetuspto-grants-2010_12
ORD IDord-6b1a4006a93549a68871622f8b84c9ff
Source noteuspto-grants-2010_12