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Water → 6-Bromo-4-hydroxy-3-phenoxyquinolin-2(1H)-one

HRID 623957
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 623957
[Br:1][C:2]1[CH:3]=[CH:4][C:5]([NH:12][C:13](=[O:22])[CH2:14][O:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)=[C:6]([CH:11]=1)[C:7](OC)=[O:8].C[Si]([N-][Si](C)(C)C)(C)C.[K+].O>O1CCCC1>[Br:1][C:2]1[CH:11]=[C:6]2[C:5](=[CH:4][CH:3]=1)[NH:12][C:13](=[O:22])[C:14]([O:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)=[C:7]2[OH:8]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 962WaterHCID 3251421Potassium bis(trimethylsilyl)amideHCID 7765744Methyl 5-bromo-2-(2-phenoxyacetamido)benzoate

Produkt 1

HCID 867154446-Bromo-4-hydroxy-3-phenoxyquinolin-2(1H)-one

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To a solution of methyl 5-bromo-2-(2-phenoxyacetamido)benzoate (7.28 g, 20.0 mmol, Intermediate 5, step a) in tetrahydrofuran (215 mL) at −78° C. was added potassium bis(trimethylsilyl)amide (0.5 M solution in toluene, 118.7 mL, 59.37 mmol) over 7 minutes. The mixture was stirred at −78° C. for 5 minutes and 0° C. for 1.5 hours. The resulting cold solution was quenched with water. The white solid formed was completely dissolved by addition of excess water. The aqueous phase was washed once with EtOAc and then acidified to pH>2 by slow addition of 2 N aqueous HCl solution. The off-white precipitate formed was filtered and dried in the air overnight and at 40° C. for 1 hour to provide the title compound.

Aufarbeitung

  1. customThe resulting cold solution was quenched with water
  2. customThe white solid formed
  3. washThe aqueous phase was washed once with EtOAc
  4. additionacidified to pH>2 by slow addition of 2 N aqueous HCl solution
  5. customThe off-white precipitate formed
  6. filtrationwas filtered
  7. customdried in the air overnight and at 40° C. for 1 hour

Quellen und Nachweise

ORD-Eintrag
ord-ed8cd9bf12084ef5b66c88c58288b968
Quelldatensatz
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09303015B2

Notizen zur Reaktion

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