HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 280772Generated: October 25, 2026
1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → dibenzylphosphoryl-L-alanyl-L-prolyl-L-alanine benzylester
https://huagongshe.com/reaction/280772
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | L-Alanine, phenylmethyl ester, 4-methylbenzenesulfonate (1:1) | HCID 2802424 | — |
| Reactant | Dibenzylphosphory-L-alanyl-L-proline | HCID 53804723 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | dibenzylphosphoryl-L-alanyl-L-prolyl-L-alanine benzylester | HCID 70042716 | — |
Reaction Steps
Dibenzylphosphoryl-L-alanyl-L-proline (1.4 g, 3.2 m mole), 1-hydroxybenzotriazol (476 mg, 3.5 m mole) and L-alanine benzylester p-toluene sulfonate (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 continued for 3 hours under cooling and then overnight at room temperature, and ethyl acetate (100 ml) was added thereto. The mixture was washed with 1N hydrochloric acid, 5% sodium bicarbonate and water in order, and dried with anhydrous sodium sulfate. The thus obtained solution was distilled under reduced pressure leaving an oily dibenzylphosphoryl-L-alanyl-L-prolyl-L-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-a4c3ab92871b4c02842e77e42db11aec |
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| Source note | uspto-grants-1986_05 |
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