HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280773Generated: October 25, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → dibenzylphosphoryl-L-alanyl-L-prolyl-D-alanine benzylester
https://huagongshe.com/reaction/280773
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | D-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1) | HCID 2802425 | — |
| Reactant | Dibenzylphosphory-L-alanyl-L-proline | HCID 53804723 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | dibenzylphosphoryl-L-alanyl-L-prolyl-D-alanine benzylester | HCID 70040519 | — |
Reaction Steps
Dibenzylphosphory-L-alanyl-L-proline (1.4 g, 3.2 m mole), HOBt (476 mg, 3.5 m mole) and D-alanine benzylester p-toluene sulfonic acid salt (1.3 g, 3.5 m mole) were dissolved in DMF (5 ml), and WSC (0.64 ml) was added thereto while cooling to -15° C. 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, 5% sodium bicarbonate and water in order. The mixture was dried with anhydrous sodium sulfate and the thus obtained solution was distilled under reduced pressure to give an oily dibenzylphosphoryl-L-alanyl-L-prolyl-D-alanine benzylester material.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04590178 |
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| Source dataset | uspto-grants-1986_05 |
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| ORD ID | ord-095c1e6ce3f2414fbfa1ba89dd751991 |
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| Source note | uspto-grants-1986_05 |
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