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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1384457Generated: November 2, 2026

HCID 70021505, compound → HCID 11056128, compound

https://huagongshe.com/reaction/1384457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 70021505HCID 70021505—
CatalystPalladium hydroxideHCID 9942167—
SolventMethanolHCID 887—
SolventEthyl AcetateHCID 8857—
ProductHCID 11056128HCID 11056128—

Reaction Steps

The crude methyl N-[(S)-1-(4-methoxyphenyl)ethyl]-3-amino-3-(3-pyridyl)propenoate, (40.6 g, 130 mmol) was dissolved in methanol (200 mL) and mixed with 20% Pd(OH)2/C (4.1 g). The mixture was hydrogenated under atmospheric pressure for 30 h. The mixture was diluted with ethyl acetate (50 mL) and filtered through celite (20 g) to remove the catalyst. The celite was washed with hot (70° C.) ethyl acetate(200 mL). The combined filtrate was concentrated under reduced pressure to near dryness to an oily residue. Crude amine (27.5 g) was dissolved in hot ethyl acetate (40 mL). The resulting hot yellow solution was filtered and rinsed with 15 mL of hot ethyl acetate. The clear solution was concentrated to <50 mL and allowed to stand at room temperature overnight. The resulting white crystalline solid was collected by filtration and washed with cold ethyl acetate (EtOAc) (˜15-20 mL), then air dried. Yield of isolated solid: 15.5 g. HPLC analysis showed >99% desired diastereomer. A second crop was obtained from the filtrate after concentration to about 20 mL. Yield: 1.7 g identical by HPLC to first crop; total yield: 17.2 g (62.5%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06258956B1
Source datasetuspto-grants-2001_07
ORD IDord-c1bd8c9a92314412a092f11314b0e5df
Source noteuspto-grants-2001_07