Triethylamine → N-(4-((3-(trifluoromethoxy)phenyl)sulfonyl)phenyl)acetamide

HRID 1754112Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1754112
[C:1]([NH:4][C:5]1[CH:10]=[CH:9][C:8]([S:11]([O-:13])=[O:12])=[CH:7][CH:6]=1)(=[O:3])[CH3:2].[Na+].[F:15][C:16]([F:28])([F:27])[O:17][C:18]1[CH:19]=[C:20](B(O)O)[CH:21]=[CH:22][CH:23]=1.CCN(CC)CC.[NH4+].[OH-]>O1CCOCC1.CS(C)=O.[Cl-].[Na+].O.CC([O-])=O.CC([O-])=O.[Cu+2].CCOC(C)=O>[F:15][C:16]([F:27])([F:28])[O:17][C:18]1[CH:23]=[C:22]([S:11]([C:8]2[CH:7]=[CH:6][C:5]([NH:4][C:1](=[O:3])[CH3:2])=[CH:10][CH:9]=2)(=[O:13])=[O:12])[CH:21]=[CH:20][CH:19]=1

Komponenten

10

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

To a solution of sodium 4-acetamidobenzenesulfinate dehydrate (128 mg, 0.5 mmol), 3-trifluoromethoxy-phenylboronic acid (144 mg, 0.75 mmol) and Et3N (0.313 mL, 2.25 mmol) in 1,4-dioxane (4 mL) and DMSO (4 mL) is added Cu(OAc)2 (114 mg, 0.625 mmol). The mixture is heated at 60° C. for 16 h then cooled to ambient temperature. EtOAc (12 ml) and brine (6 ml) is added followed by concentrated NH4OH (0.6 mL) and the mixture is stirred at ambient temperature for 15 min. The layers are separated and the aqueous layer is extracted with EtOAc (6 mL). The combined extracts are dried (Na2SO4) and evaporated. The residue is purified by preparative TLC with 2:1 EtOAc/hexanes to give 104 mg (57%) white solid.

Aufarbeitung

  1. temperaturethen cooled to ambient temperature
  2. customThe layers are separated
  3. extractionthe aqueous layer is extracted with EtOAc (6 mL)
  4. dry with materialThe combined extracts are dried (Na2SO4)
  5. customevaporated
  6. customThe residue is purified by preparative TLC with 2:1 EtOAc/hexanes

Quellen und Nachweise

ORD-Eintrag
ord-8008021cc14c4081b4213b819b0bdec4
Quelldatensatz
uspto-grants-2015_10
Patentnummer
US09169209B2

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