HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 651830Generated: November 3, 2026
O-Benzylhydroxylamine → HCID 86757338, compound
https://huagongshe.com/reaction/651830
Participants
| Role | Name | HCID | Charge |
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| Reactant | O-Benzylhydroxylamine | HCID 102313 | — |
| Reactant | HCID 70202725 | HCID 70202725 | — |
| Catalyst | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86757338 | HCID 86757338 | 32.9% |
Reaction Steps
A solution of 0.151 g of 2(R)-[1(S)-(carboxy)-4-phenylbutyl]-N-[3-[2-(dimethylamino)ethyl]-2,5-dioxo-1-imidazolidinyl]-4-methylvaleramide and 0.157 g of O-benzylhydroxylamine in 0.25 ml of dimethylformamide was treated with 0.054 mg of 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride and stirred at room temperature for 4 hours. The mixture was diluted with ethyl acetate and washed with 5% aqueous sodium hydrogen carbonate and saturated aqueous sodium chloride. The organic layer was dried over anhydrous magnesium sulfate and evaporated to give a residue which was purified by flash column chromatography on silica gel, using methanol/dichloromethane (5:95) for the elution, to give 0.061 g of 2(R)-[1(S)-(benzyloxycarbamoyl)-4-phenylbutyl]-N-[3-[2-(dimethylamino)ethyl]-2,5-dioxo-1-imidazolidinyl]-4-methylvaleramide in the form of a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06281363B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-ed17db1815ed4acf917c58e7c213dd41 |
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| Source note | uspto-grants-2001_08 |
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