HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1601021Generated: October 28, 2026
1-Hydroxybenzotriazole → HCID 57128097, compound
https://huagongshe.com/reaction/1601021
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | trans-4-Hydroxy-1-(4-nitrobenzyloxycarbonyl)-L-proline | HCID 10566895 | — |
| Reactant | HCID 70100666 | HCID 70100666 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 57128097 | HCID 57128097 | 99.1% |
Reaction Steps
To a solution of (2S,4R)-4-hydroxy-1-(4-nitrobenzyloxycarbonyl)proline (4.65 g) in anhydrous dimethylformamide (60 ml), (3S)-3-[N-methyl-N-(4-nitrobenzyloxycarbonyl)aminomethyl]pyrrolidine hydrochloride (4.95 g), diisopropylethylamine (5.23 ml), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (4.03 g) and 1-hydroxybenzotriazole (2.23 g) were added. The resulting mixture was stirred at room temperature for 10 hours. The reaction mixture was concentrated by evaporation under reduced pressure. The residue was dissolved in ethyl acetate. The resulting solution was washed with water and the organic layer was dried over anhydrous sodium sulfate. The solvent was distilled off and the residue was subjected to chromatography through a silica gel column. From the fractions eluted with ethyl acetate/methanol=9/1, (2S,4R)-4-hydroxy-2-[(3S)-3-[N-methyl-N-(4-nitrobenzyloxycarbonyl)aminomethyl]pyrrolidin-1-ylcarbonyl]-1-(4-nitrobenzyloxycarbonyl)pyrrolidine (8.70 g) was obtained as a powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05977097 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-9dbdf6ffac0b4c3381768545c43b3d61 |
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| Source note | uspto-grants-1999_11 |
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