Bromoacetone → 2-Methoxy-5-[(4-methyl-1,3-thiazol-2-yl)amino]phenol
Reaktionsgleichung
[OH:1][C:2]1[CH:3]=[C:4]([NH:10][C:11]([NH2:13])=[S:12])[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].Br[CH2:15][C:16](=O)[CH3:17]>CN(C=O)C>[CH3:9][O:8][C:7]1[CH:6]=[CH:5][C:4]([NH:10][C:11]2[S:12][CH:15]=[C:16]([CH3:17])[N:13]=2)=[CH:3][C:2]=1[OH:1]Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Following the general procedure for the synthesis of derivatives 6 and 7, a solution of 1-(3-hydroxy-4-methoxyphenyl)thiourea (100 mg, 0.50 mmol) and bromoacetone (83 mg, 0.60 mmol) in dry DMF (2.0 mL) was heated at 60° C. for 6 h. The title compound was obtained after purification by flash chromatography on silica gel (hexane:EtOAc 6/4) in 26% yield (30 mg).
Aufarbeitung
- customfor the synthesis of derivatives 6 and 7
Quellen und Nachweise
- ORD-Eintrag
- ord-68af7d98a7bb4f3fb4c4fd61771b711a
- Quelldatensatz
- uspto-grants-2015_04
- Patentnummer
- US09018209B2
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