Water → HCID 59316492, Verbindung

HRID 471861

Reaktionsgleichung

Br[C:2]1[CH:3]=[C:4]([CH:8]=[CH:9][CH:10]=1)[C:5]([NH2:7])=[O:6].[F:11][C:12]1[CH:13]=[C:14](B(O)O)[CH:15]=[CH:16][C:17]=1[CH:18]=[O:19].C([O-])([O-])=O.[K+].[K+].O>[Br-].C([N+](CCCC)(CCCC)CCCC)CCC.CC([O-])=O.CC([O-])=O.[Pd+2].CCOCC>[F:11][C:12]1[CH:13]=[C:14]([C:2]2[CH:10]=[CH:9][CH:8]=[C:4]([C:5]([NH2:7])=[O:6])[CH:3]=2)[CH:15]=[CH:16][C:17]=1[CH:18]=[O:19]

Komponenten

Reaktionsbedingungen

Temperatur: 80 °C

Versuchsvorschrift

A 10 mL conical vial equipped with magnetic spin vane was charged with 3-bromobenzamide (0.200 g; 1.00 mmol; Ex IV-6), 3-fluoro-4-formyl-phenyl boronic acid (0.185 g; 1.1 mmol), tetra-n-butyl ammonium bromide (0.323 g; 1.0 mmol), Pd(OAc)2 (0.0011 g; 0.005 mmol), K2CO3 (0.345 g; 2.5 mmol) and sealed with a septum. The vial was evacuated/backfilled with nitrogen (×3), water was added via syringe and the mixture was stirred at 80° C. for 2.5 h. Upon cooling, the mixture was poured into water, layered with Et2O and sonicated ca. 2 min. Solid was collected by filtration and washed with Et2O, affording the title compound as a cream-colored solid (used without further purification). LC/MS (method A) 2.02 min; m/z 244 (M+H).

Aufarbeitung

customA 10 mL conical vial equipped with magnetic spin vane
customsealed with a septum
additionwas added via syringe
temperatureUpon cooling
customsonicated ca. 2 min
filtrationSolid was collected by filtration
washwashed with Et2O

Quellen und Nachweise

ORD-Eintrag: ord-e2f444bf2a2b43de82391a737fce323e
Quelldatensatz: uspto-grants-2014_01
DOI: 10.6084/m9.figshare.5104873.v1
Patentnummer: US08633175B2

Verknüpfte Notizen

Wird geladen…