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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454111Generated: November 2, 2026

Potassium Carbonate → ethyl (alphaS)-alpha-[[(1,1-dimethylethoxy)carbonyl]amino]-4'-ethoxymethyl-2',6'-dimethoxy(1,1'-biphenyl)-4-propionate

https://huagongshe.com/reaction/1454111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantTriphenylphosphineHCID 11776—
Reactant(4-(Ethoxymethyl)-2,6-dimethoxyphenyl)boronic acidHCID 10236170—
ReactantN-Boc-4-bromo-L-phenylalanine ethyl esterHCID 69597080—
Catalystpalladium(II) acetateHCID 167845—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Productethyl (alphaS)-alpha-[[(1,1-dimethylethoxy)carbonyl]amino]-4'-ethoxymethyl-2',6'-dimethoxy(1,1'-biphenyl)-4-propionateHCID 11329259139.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

Under nitrogen atmosphere, a mixture of ethyl (αS)-α-[[(1,1-dimethylethoxy)carbonyl]amino]-4-bromobenzene propanoate (11.17 g), 4-ethoxymethyl-2,6-dimethoxyphenylboronic acid (10.80 g), palladium acetate (0.34 g), triphenylphosphine (1.57 g), anhydrous potassium carbonate (12.44 g), N-methylpyrrolidone (56 ml) and water (11 ml) was stirred for 50 minutes at 80° C. After completion of the reaction, the mixture was cooled to room temperature and extracted with ethyl acetate and water. The organic layer was washed with 10% aqueous citric acid solution and saturated aqueous NaCl solution, dried over magnesium sulfate and filtrated. The filtrate was concentrated under reduced pressure to yield ethyl (αS)-α-[[(1,1-dimethylethoxy)carbonyl]amino]-4′-ethoxymethyl-2′,6′-dimethoxy(1,1′-biphenyl)-4-propionate (20.4 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07476758B2
Source datasetuspto-grants-2009_01
ORD IDord-9897b36671f44fc89a04441963d359a2
Source noteuspto-grants-2009_01