HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1468312Erstellt: 27. Oktober 2026
Dimethylformamide → O-{[(3-sulfophenyl)amino]carbonyl}-L-serine
https://huagongshe.com/reaction/1468312
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dimethylformamide | HCID 6228 | — |
| Edukt | 3-Aminobenzenesulfonic acid | HCID 8474 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Boc-Ser-Otbu | HCID 7019054 | — |
| Lösungsmittel | Dichloromethane | HCID 6344 | — |
| Lösungsmittel | Trifluoroacetic acid | HCID 6422 | — |
| Produkt | O-{[(3-sulfophenyl)amino]carbonyl}-L-serine | HCID 45275682 | 0,6% |
Reaktionsschritte
Boc-Ser-OtBu (200 mg, 0.77 mmol) was dissolved in 3 ml of methylene chloride and cooled to 0° C. N,N′-carbonyldiimidazole (124 mg, 0.77 mmol) was added to the solution and stirred at room temperature for 2 hours. After the solvent was removed by distillation, 3-aminobenzenesulfonic acid (132.6 mg, 0.77 mmol), 2 ml of DMF and 0.4 ml of diisopropylethylamine were added and stirred at 70° C. overnight. The solvent was removed by distillation and the mixture was purified according to the purification step A to give the intermediate. The resulting intermediate was dissolved in 1 ml of TFA and stirred at room temperature for 2 hours. The solvent was removed by distillation, and the mixture was purified according to the purification step A to give the title compound.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US09000208B2 |
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| Quelldatensatz | uspto-grants-2015_04 |
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| ORD ID | ord-54d0111145614fddaee480a926d687a3 |
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| Quellennotiz | uspto-grants-2015_04 |
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