HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1874577Erstellt: 26. Oktober 2026
Iodoacetamide → N-{3-[(1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl)oxy]phenyl}-3-(1-cyanocyclopropyl)benzamide
https://huagongshe.com/reaction/1874577
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Iodoacetamide | HCID 3727 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 3-(1-cyanocyclopropyl)-N-{3-[(6-{[(4-methylphenyl)sulfonyl]amino}pyridin-3-yl)oxy]phenyl}benzamide | HCID 68417875 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | N-{3-[(1-(2-amino-2-oxoethyl)-6-{[(4-methylphenyl)sulfonyl]imino}-1,6-dihydropyridin-3-yl)oxy]phenyl}-3-(1-cyanocyclopropyl)benzamide | HCID 68416709 | 77,1% |
Reaktionsschritte
To a solution of 3-(1-cyanocyclopropyl)-N-{3-[(6-{[(4-methylphenyl)sulfonyl]amino}pyridin-3-yl)oxy]phenyl}benzamide (2.5 g, 4.77 mmol) in N,N-dimethylformamide (15 mL) was added N,N-diisopropylethylamine (0.90 mL, 5.01 mmol), and the mixture was stirred at room temperature for 15 min. 2-Iodoacetamide (927 mg, 5.01 mmol) was added to the reaction mixture, and the mixture was stirred at room temperature for 48 hr. The reaction mixture was concentrated under reduced pressure, water (150 mL) was added to the residue, and the mixture was extracted with ethyl acetate (150 mL). The organic layer was washed with saturated brine (150 mL) and dried over anhydrous magnesium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was recrystallized from ethyl acetate and hexane to give the title compound (2.14 g, 77%) as a pale-yellow solid.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08304557B2 |
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| Quelldatensatz | uspto-grants-2012_11 |
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| ORD ID | ord-11765431a5cb4771bfa262a371bcb46b |
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| Quellennotiz | uspto-grants-2012_11 |
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