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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563193Erstellt: 24. Oktober 2026

m-Hydroxybenzohydrazide → N'-((2R,3R)-2-(3-chloro-1-cyano-2-methylphenylamino)-3-hydroxybutanoyl)-3-hydroxy-benzohydrazide

https://huagongshe.com/de/reaction/563193

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-HydroxybenzohydrazideHCID 79889—
Edukt(2R,3R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acidHCID 57908625—
EduktN'-((2R,3S)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoyl)benzohydrazideHCID 67006523—
LösungsmittelEthylacetate methanolHCID 21584119—
ProduktN'-((2R,3R)-2-(3-chloro-1-cyano-2-methylphenylamino)-3-hydroxybutanoyl)-3-hydroxy-benzohydrazideHCID 67006932—

Reaktionsschritte

(2R,3R)-2-(3-chloro-4-cyano-2-methylphenylamino)-3-hydroxybutanoic acid (663 mg, 2.5 mmol) (intermediate 3a) and 3-hydroxy-benzohydrazide (376 mg, 2.5 mmol) were coupled similarly to the procedure used for intermediate 1b. After column chromatography (5% methanol/EtOAc) the title compound was isolated as a white solid (615 mg, 62%). 1H NMR (500 MHz, acetone-d6, δ in ppm) 9.79 (br s, 1H), 8.81 (br s, 1H), 7.45 (ad, J=8.7 Hz, 1H), 7.38 (m, 2H), 7.27 (t, J=7.87 Hz, 1H), 7.02 (m, 1H), 6.71 (d, J=8.7 Hz, 1H), 5.61 (m, 1H), 4.23 (m, 1H), 4.14 (m, 1H), 2.29 (s, 3H), 1.37 (d, J=6.5 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067448B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-caf082e460f14d0c98bc58e820515990
Quellennotizuspto-grants-2011_11