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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 485574Generated: October 25, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → dibenzylphosphoryl-L-alanyl-L-prolyl-L-tyrosine ethylester

https://huagongshe.com/reaction/485574

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantTyrosine ethyl ester hydrochlorideHCID 2724939—
ReactantDibenzylphosphory-L-alanyl-L-prolineHCID 53804723—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productdibenzylphosphoryl-L-alanyl-L-prolyl-L-tyrosine ethylesterHCID 7004048079.8%

Reaction Conditions

Temperature-15 °C

Reaction Steps

Dibenzylphosphoryl-L-alanyl-L-proline (1.2 g, 2.5 m mole), HOBt (338 mg, 2.5 m mole) and L-tyrosine ethylester hydrochloride (737 mg, 3 m mole) was suspended in DMF (10 ml), and WSC (0.5 ml) was added gradually thereto while cooling to -15° C. and stirring. The reaction was carried out for 3 hours under cooling and then overnight at room temperature. To the reaction solution ethyl acetate (100 ml) was added, and the mixture was washed with 1N hydrochloric acid and water in order, and dried with anhydrous sodium sulfate. The solvent was removed by distillation under reduced pressure to obtain an oily dibenzylphosphoryl-L-alanyl-L-prolyl-L-tyrosine ethylester (1.4 g). This oily material gave a single spot with Rf 0.50 by thin layer chromatography (developing solvent; chloroform:methanol:acetic acid=95:5:3, colour forming method: spraying of 25% hydrobromic acid and 0.1% ninhydrine, and heating).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04536395
Source datasetuspto-grants-1985_08
ORD IDord-4f3b6450fbb347909164d5c69ba4fc33
Source noteuspto-grants-1985_08