Diisopropylethylamine → HCID 59322424, Verbindung
Reaktionsgleichung
Cl.Cl.Cl.[F:4][C:5]1[CH:6]=[C:7]([C:12]2[N:13]=[C:14]([CH:22]3[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]3)[N:15]([CH:17](N(C)C)[CH3:18])[CH:16]=2)[CH:8]=[CH:9][C:10]=1[F:11].Cl[C:29]1[N:37]=[CH:36][N:35]=[C:34]2[C:30]=1[N:31]([CH3:39])[C:32](=[O:38])[NH:33]2.C[CH2:41][N:42](C(C)C)[CH:43](C)C>CN1C(=O)CCC1>[F:4][C:5]1[CH:6]=[C:7]([C:12]2[N:13]=[C:14]([CH:22]3[CH2:23][CH2:24][N:25]([C:29]4[N:37]=[CH:36][N:35]=[C:34]5[C:30]=4[N:31]([CH3:39])[C:32](=[O:38])[NH:33]5)[CH2:26][CH2:27]3)[N:15]([CH2:17][CH2:18][N:42]([CH3:43])[CH3:41])[CH:16]=2)[CH:8]=[CH:9][C:10]=1[F:11]Komponenten
5
Edukt 3
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
Combine 2-(4-(3,4-difluorophenyl)-2-(piperidin-4-yl)-1H-imidazol-1-yl-N,N-dimethyl ethanamine 3HCl (0.3 g; 0.00068 mol), 6-chloro-7-methyl-7,9-dihydro-purin-8-one (0.15 g; 0.00081 mol), DIPEA (1.07 mL; 0.0062 mol) in NMP (9 mL) and stir at 150° C. in microwave for 45 min. Cool, and quench the reaction with saturated sodium bicarbonate solution and extract with EA. Evaporate the EA layer and purify on silica gel using DCM and methanol as eluent to give the title compound (0.032 g; 9.3%). MS (ES+): m/z=484 (M+1).
Aufarbeitung
- temperatureCool
- customquench
- customthe reaction with saturated sodium bicarbonate solution
- extractionextract with EA
- customEvaporate the EA layer
- custompurify on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-8599121dea23456988af40db8080f49c
- Quelldatensatz
- uspto-grants-2012_04
- Patentnummer
- US08148387B2
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