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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktHydroxyamine hydrochlorideHCID 443297—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
EduktE-3-chloro-4-hydroxyphenylcinnamic acidHCID 68583309—
LösungsmittelDimethylformamideHCID 6228—
ProduktE-3-[3'-chloro-4'-hydroxybiphenyl-4-yl]-N-hydroxy-acrylamideHCID 159865079,7%

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07728039B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-4f92bbdf0eb249bf94c24643ff3d3a30
Quellennotizuspto-grants-2010_06