HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16656Erstellt: 23. Oktober 2026
1-Hydroxybenzotriazole → Tert-butyl 2-[3-{1-(4-sulfamoylphenyl)-5-p-tolyl-1h-pyrazol-3-yl}propanamido]ethylcarbamate
https://huagongshe.com/de/reaction/16656
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | N-BOC-ethylenediamine | HCID 187201 | — |
| Edukt | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Edukt | Celecox Sulforhodamine | HCID 131728181 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | Tert-butyl 2-[3-{1-(4-sulfamoylphenyl)-5-p-tolyl-1h-pyrazol-3-yl}propanamido]ethylcarbamate | HCID 66813400 | 46% |
Reaktionsschritte
a Celecox-Sulforhodamine Analog: Compound 30f was synthesized by the method outlined in FIG. 3. Briefly, Compound 30c as synthesized as set forth hereinabove. Compound 30c was then complexed with tert-butyl 2-aminoethylcarbamate for 16 hours at room temperature in the presence of 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide hydrochloride (EDCl), 1-hydroxybenzotriazole (HOBt), and N,N-diisopropylethylamine (DIPEA) in mimethylformamide (DMF) to produce tert-butyl 2-[3-{1-(4-sulfamoylphenyl)-5-p-tolyl-1H-pyrazol-3-yl}propanamido]ethylcarbamate as a yellow solid (46% yield). This product was then dissolved in dichloromethane and treated with HCl (gas) for 2 hours at room temperature, producing N-(2-aminoethyl)-3-{1-(4-sulfamoylphenyl)-5-p-tolyl-1H-pyrazol-3-yl}propanamide hydrochloride as a yellow solid (80% yield).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07736624B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-de5eb08e7d1e4c42908d8980e52fde1c |
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| Quellennotiz | uspto-grants-2010_06 |
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