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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2418507Generated: November 4, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → dibenzylphosphoryl-L-alanyl-L-prolyl-glycine benzylester

https://huagongshe.com/reaction/2418507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-benzylglycine toluene-p-sulphonateHCID 6451311—
ReactantDibenzylphosphory-L-alanyl-L-prolineHCID 53804723—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Productdibenzylphosphoryl-L-alanyl-L-prolyl-glycine benzylesterHCID 7004263892.2%

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 glycine benzylester p-toluene sulfonic acid salt (1.0 g, 3 m mole) were suspended in DMF (10 ml), and WSC (0.5 ml) was dropwise added thereto while cooling to -15° C. and stirring. The reaction was carried out for 3 hours under cooling, and next, 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 thus dried solution was distilled under reduced pressure to give an oily dibenzylphosphoryl-L-alanyl-L-prolyl-glycine benzylester material (1.5 g). The oily material gave a single spot with Rf 0.7 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 numberUS04472381
Source datasetuspto-grants-1984_09
ORD IDord-50ad5953318146b6b6615d8d0f22187e
Source noteuspto-grants-1984_09