N-Methoxy-N-methyl-2-phenylacetamide → HCID 66665381, Verbindung

HRID 872298Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 872298
Br[C:2]1[CH:7]=[CH:6][C:5]([C:8]23[CH2:14][CH:12]([CH2:13]2)[O:11][C:10](=[O:15])[NH:9]3)=[CH:4][CH:3]=1.[Li]CCCC.CON(C)[C:24](=[O:32])[CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>C1COCC1.CCCCCC>[C:26]1([CH2:25][C:24]([C:2]2[CH:7]=[CH:6][C:5]([C:8]34[CH2:14][CH:12]([CH2:13]3)[O:11][C:10](=[O:15])[NH:9]4)=[CH:4][CH:3]=2)=[O:32])[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1

Komponenten

6

Versuchsvorschrift

A solution of 5-(4-bromo-phenyl)-2-oxa-4-aza-bicyclo[3.1.1]heptan-3-one (prepared according to WO2009/148916, 4 g) in dry THF (60 mL) was cooled to −78° C. and treated with n-BuLi (6.56 mL of a 2.5M solution in hexane) and stirred for 30 minutes at this temperature before addition of further n-BuLi (13.1 mL of a 2.5M solution in hexane). Stirring was continued at this temperature for 30 minutes before a solution of N-methoxy-N-methyl-benzeneacetamide (prepared according to US6407119B1, 4.6 g) in THF (10 mL) was added. After 10 minutes the reaction was quenched with saturated aqueous ammonium chloride solution, extracted with EtOAc and the combined organic phases washed with brine, filtered and concentrated. The residue was triturated with hexane/EtOAc to give the title compound which was used in the next step without further purification.

Aufarbeitung

  1. additionwas added
  2. customAfter 10 minutes the reaction was quenched with saturated aqueous ammonium chloride solution
  3. extractionextracted with EtOAc
  4. washthe combined organic phases washed with brine
  5. filtrationfiltered
  6. concentrationconcentrated
  7. customThe residue was triturated with hexane/EtOAc

Quellen und Nachweise

ORD-Eintrag
ord-390350192f2947f3b4acc0ccb2377f88
Quelldatensatz
uspto-grants-2015_03
Patentnummer
US08975265B2

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