HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 546584Erstellt: 26. Oktober 2026
1-Pyrrolidinepropanamine → 1-(4-{[3-(4-Tert-butylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl]methyl}pyridin-2-yl)-3-(3-pyrrolidin-1-ylpropyl)urea
https://huagongshe.com/reaction/546584
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | 1-Pyrrolidinepropanamine | HCID 31670 | — |
| Edukt | 3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dione | HCID 57625975 | — |
| Lösungsmittel | Dimethyl Sulfoxide | HCID 679 | — |
| Lösungsmittel | Water | HCID 962 | — |
| Produkt | 1-(4-{[3-(4-Tert-butylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl]methyl}pyridin-2-yl)-3-(3-pyrrolidin-1-ylpropyl)urea | HCID 57626000 | 15,1% |
Reaktionsschritte
To a solution of 100 mg of 3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dione obtained in stage b) below in 2 mL of dimethyl sulphoxide are added 120 mg of 3-pyrrolidin-1-ylpropan-1-amine. The solution is stirred at a temperature of 100° C. for 1 hour 40 minutes. After cooling to a temperature in the region of 20° C., the reaction medium is diluted with water, the suspension is filtered and the precipitate is purified by chromatography on a column of silica, eluting with a dichloromethane/methanol/28% aqueous ammonia mixture (gradient from 100/0 to 75/20/5 by volume). 18.5 mg of 1-(4-{[3-(4-tert-butylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl]methyl}pyridin-2-yl)-3-(3-pyrrolidin-1-ylpropyl)urea are obtained in the form of a pale yellow powder, the characteristics of which are as follows:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07935819B2 |
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| Quelldatensatz | uspto-grants-2011_05 |
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| ORD ID | ord-dc8ebb03c0744150885449c27609e79f |
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| Quellennotiz | uspto-grants-2011_05 |
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