(S)-2-(2-Nitro-phenylamino)-propionic acid tert-butyl ester → (S)-2-(2-Amino-phenylamino)-propionic acid tert-butyl ester

HRID 1747386Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1747386
[C:1]([O:5][C:6](=[O:19])[C@@H:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[N+:16]([O-])=O)[CH3:8])([CH3:4])([CH3:3])[CH3:2]>CO.[Pd]>[C:1]([O:5][C:6](=[O:19])[C@@H:7]([NH:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=1[NH2:16])[CH3:8])([CH3:2])([CH3:3])[CH3:4]

Komponenten

4

Edukt 1

HCID 59497415(S)-2-(2-Nitro-phenylamino)-propionic acid tert-butyl ester

Produkt 1

HCID 59497437(S)-2-(2-Amino-phenylamino)-propionic acid tert-butyl esterAusbeute 105,8 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 23938PalladiumKatalysatorHCID 887MethanolLösungsmittel

Versuchsvorschrift

To a solution of (S)-2-(2-Nitro-phenylamino)-propionic acid tert-butyl ester (1.6 g, 6.0 mmol) in MeOH (20 mL) was added a slurry of 10% Pd/C (dry) (300 mg). The reaction mixture was degasses using house vacuum aspirator and then saturated with H2 gas in balloon. The reaction mixture was stirred at room temperature for 16 h. The reaction mixture was then filtered through a celite and the filtrate was concentrated to afford 1.5 g (100%) of the desired product as a dark brown oily residue. This product was used for the next reaction without purification.

Aufarbeitung

  1. filtrationThe reaction mixture was then filtered through a celite
  2. concentrationthe filtrate was concentrated

Quellen und Nachweise

ORD-Eintrag
ord-d68b5dac7c4546a0829b4defaeedd18c
Quelldatensatz
uspto-grants-2015_10
Patentnummer
US09150556B2

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