tert-Butoxy bis(dimethylamino)methane → HCID 53847223, Verbindung
Reaktionsgleichung
[Br:1][C:2]1[CH:17]=[CH:16][C:5]([C:6]([C:8]2[CH:9]=[CH:10][C:11](=[O:15])[NH:12][C:13]=2[CH3:14])=[O:7])=[CH:4][CH:3]=1.[CH3:18][N:19]([CH:21](N(C)C)OC(C)(C)C)[CH3:20]>O1CCOCC1>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([C:8]2[CH:9]=[CH:10][C:11](=[O:15])[NH:12][C:13]=2[CH:14]=[CH:18][N:19]([CH3:21])[CH3:20])=[O:7])=[CH:16][CH:17]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
m.p. 265°-268° C. with decomposition, 53.8 g, was prepared following the procedure described in Example B-2 using 44 g of 5-(4-bromobenzoyl)-6-methyl-2(1H)-pyridinone, 300 ml of p-dioxane and 35 ml of bis-(dimethylamino)-t-butoxymethane.
Aufarbeitung
- customm.p. 265°-268° C. with decomposition, 53.8 g, was prepared
Quellen und Nachweise
- ORD-Eintrag
- ord-7f7794d30b2b4a3290a99ef9484fbc0a
- Quelldatensatz
- uspto-grants-1985_12
- Patentnummer
- US04560691
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