(S)-1-Hydrazino-butan-2-ol → (S)-1-[5-(2-Chloro-6-methyl-pyridin-4-yl)-3-(3,4-difluoro-phenylamino)-[1,2,4]triazol-1-yl]-butan-2-ol
Reaktionsgleichung
[Cl:1][C:2]1[CH:7]=[C:6]([C:8]([NH:10][C:11](=[N:14][C:15]2[CH:20]=[CH:19][C:18]([F:21])=[C:17]([F:22])[CH:16]=2)SC)=O)[CH:5]=[C:4]([CH3:23])[N:3]=1.[NH:24]([CH2:26][C@@H:27]([OH:30])[CH2:28][CH3:29])[NH2:25]>CC(O)(C)C>[Cl:1][C:2]1[CH:7]=[C:6]([C:8]2[N:24]([CH2:26][C@@H:27]([OH:30])[CH2:28][CH3:29])[N:25]=[C:11]([NH:14][C:15]3[CH:20]=[CH:19][C:18]([F:21])=[C:17]([F:22])[CH:16]=3)[N:10]=2)[CH:5]=[C:4]([CH3:23])[N:3]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Intermediate D2 (1 g; 2.81 mmol) was dissolved in t-BuOH (40 ml) and, then intermediate D3 (0.44 g; 4.22 mmol) was added. The reaction mixture was stirred and refluxed for 4 hours and then the solvent was evaporated. The residue was purified by silica column chromatography (gradient: CH2Cl2/10% CH3OH in CH2Cl2 from 100/0 to 0/100). Yield: 1.1 g of intermediate D4 (S-enantiomer).
Aufarbeitung
- temperaturerefluxed for 4 hours
- customthe solvent was evaporated
- customThe residue was purified by silica column chromatography (gradient: CH2Cl2/10% CH3OH in CH2Cl2 from 100/0 to 0/100)
Quellen und Nachweise
- ORD-Eintrag
- ord-5cad52bd32f44315ac6e48f044a984ec
- Quelldatensatz
- uspto-grants-2013_05
- Patentnummer
- US08440701B2
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