Reaktionsgleichung
[CH3:1][C@@H:2]1[CH2:7][CH2:6][CH2:5][N:4]([C:8](=[O:22])[C:9]2[CH:14]=[C:13]([CH3:15])[CH:12]=[CH:11][C:10]=2[C:16]2[CH:17]=[N:18][N:19]([CH3:21])[CH:20]=2)[C@@H:3]1[CH2:23][N:24]1C(=O)C2C(=CC=CC=2)C1=O.O.NN>CO>[NH2:24][CH2:23][C@@H:3]1[C@H:2]([CH3:1])[CH2:7][CH2:6][CH2:5][N:4]1[C:8]([C:9]1[CH:14]=[C:13]([CH3:15])[CH:12]=[CH:11][C:10]=1[C:16]1[CH:17]=[N:18][N:19]([CH3:21])[CH:20]=1)=[O:22]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 60 °C
Versuchsvorschrift
A mixture of 2-(((2S,3R)-3-methyl-1-(5-methyl-2-(1-methyl-1H-pyrazol-4-yl)benzoyl)piperidin-2-yl)methyl)isoindoline-1,3-dione (0.67 g, 1.5 mmol) and hydrazine hydrate (0.46 g, 9.27 mmol) in MeOH (10 mL) was heated at 60° C. for 2 h. The mixture was cooled to rt and the solvent was removed in vacuo. The crude was dissolved in EtOAc and washed with 2 N NaOH (2×), brine, and then dried (Na2SO4). The solvent was removed in vacuo to obtain the title compound which was used without further purification. ESI-MS (m/z): 327 [M+1]+.
Aufarbeitung
- temperatureThe mixture was cooled to rt
- customthe solvent was removed in vacuo
- dissolutionThe crude was dissolved in EtOAc
- washwashed with 2 N NaOH (2×), brine
- dry with materialdried (Na2SO4)
- customThe solvent was removed in vacuo
Quellen und Nachweise
- ORD-Eintrag
- ord-4e3bd81d2a5b4d49bed37df63cd49eb6
- Quelldatensatz
- uspto-grants-2016_09
- Patentnummer
- US09440982B2
Verknüpfte Notizen
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