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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 896713Generated: October 28, 2026

HCID 22349896, compound → HCID 22349880, compound

https://huagongshe.com/reaction/896713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22349896HCID 22349896—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 22349880HCID 2234988088.5%

Reaction Steps

Methyl 4′-(1-{[(benzyloxy)carbonyl]amino}-1-methylethyl)-3-fluoro-1,1′-biphenyl-2-carboxylate (0.25 g, 0.59 mmol) was dissolved in 6.0 mL of anhydrous ethanol. Pd/C (90 mg) was then added and the nitrogen atmosphere was exchanged for hydrogen. The reaction mixture was allowed to stir for 72 hours. After filtration though celite, the ethanol was removed under reduced pressure to yield 0.15 grams of methyl 4′-(1-amino-1-methylethyl)-3-fluoro-1,1′-biphenyl-2-carboxylate which was of sufficient purity to use directly in the next reaction.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06919343B2
Source datasetuspto-grants-2005_07
ORD IDord-b5bd335bdbb54389b61a01cd83c742b0
Source noteuspto-grants-2005_07