HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 12989Erstellt: 24. Oktober 2026
Diisopropylethylamine → E-3-[3'-chloro-4'-hydroxybiphenyl-4-yl]-N-hydroxy-acrylamide
https://huagongshe.com/de/reaction/12989
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | Hydroxyamine hydrochloride | HCID 443297 | — |
| Edukt | Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) | HCID 9886157 | — |
| Edukt | E-3-chloro-4-hydroxyphenylcinnamic acid | HCID 68583309 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | E-3-[3'-chloro-4'-hydroxybiphenyl-4-yl]-N-hydroxy-acrylamide | HCID 15986507 | 9,7% |
Reaktionsschritte
205 mg (0.75 mmol) of E-3-chloro-4-hydroxyphenylcinnamic acid were dissolved under nitrogen in 7.5 ml of DMF, then 285 mg (0.75 mmol) of HATU and 97 μL (0.56 mmol) of DIPEA were added and the solution thus obtained was kept under stirring at room temperature for 2 min. After addition of hydroxylamine hydrochloride (261 mg, 3.75 mmol), the mixture was stirred at room temperature for 2 days. DMF was removed under reduced pressure and the residue was washed with water to obtain, after filtration, 140 mg of a crude product. Purification by flash chromatography on reverse phase ((LiChroprep RP-18, MERCK) using as eluent water/methanol 1:1 and crystallization from diethyl ether afforded 21 mg of the title compound as a white solid. M.p. 172-175° C. Rf=0.16 (RP18 MERCK, H2O/MeOH 1:1).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07728039B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-4f92bbdf0eb249bf94c24643ff3d3a30 |
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| Quellennotiz | uspto-grants-2010_06 |
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