Reaktionsgleichung
[CH2:1]([O:5][C:6]1[CH:14]=[CH:13][C:9]([C:10]([OH:12])=O)=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH3:4].[B-](F)(F)(F)F.CCOC(C(C#N)=NOC(N(C)C)=[N+](C)C)=O.C(N(CC)C(C)C)(C)C.[CH3:46][N:47]([CH3:63])[CH:48]1[CH2:52][CH2:51][N:50]([C:53]2[CH:62]=[CH:61][C:56]([C:57]([NH:59][NH2:60])=[O:58])=[CH:55][CH:54]=2)[CH2:49]1>O.CN(C=O)C>[CH2:1]([O:5][C:6]1[CH:7]=[CH:8][C:9]([C:10]([NH:60][NH:59][C:57](=[O:58])[C:56]2[CH:55]=[CH:54][C:53]([N:50]3[CH2:51][CH2:52][CH:48]([N:47]([CH3:46])[CH3:63])[CH2:49]3)=[CH:62][CH:61]=2)=[O:12])=[CH:13][CH:14]=1)[CH2:2][CH2:3][CH3:4]Komponenten
7
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 2
Versuchsvorschrift
A mixture of 4-butoxybenzoic acid (156 mg) and DMF (10 ml) was mixed with TOTU (264 mg) and N,N-diisopropylethylamine (104 mg). After 10 minutes, 4-(3-dimethylaminopyrrolidin-1-yl)benzohydrazide (200 mg) was added. After one hour, the mixture was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, dried over magnesium sulfate, filtered and concentrated. The product with the molecular weight of 424.55 (C24H32N4O3) was obtained in this way; MS (ESI): 425 (M+H+).
Aufarbeitung
- waitAfter one hour
- extractionextracted with ethyl acetate
- washThe organic phase was washed with water
- dry with materialdried over magnesium sulfate
- filtrationfiltered
- concentrationconcentrated
- customThe product with the molecular weight of 424.55 (C24H32N4O3) was obtained in this way
Quellen und Nachweise
- ORD-Eintrag
- ord-90a1953210df42a280c8aad24f8dcf72
- Quelldatensatz
- uspto-grants-2008_01
- Patentnummer
- US07319108B2
Verknüpfte Notizen
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