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Ammonia → 6-chloro-3-methyl-3,4-dihydro-2H-isoquinolin-1-one

HRID 2277585
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2277585
C[O:2][C:3](=O)[NH:4][CH:5]([CH3:14])[CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[C:9]([Cl:13])[CH:8]=1.N>>[Cl:13][C:9]1[CH:8]=[C:7]2[C:12](=[CH:11][CH:10]=1)[C:3](=[O:2])[NH:4][CH:5]([CH3:14])[CH2:6]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

3

Edukt 2

HCID 222AmmoniaHCID 86685920[2-(3-Chloro-phenyl)-1-methyl-ethyl]-carbamic acid methyl ester

Produkt 1

HCID 866859216-chloro-3-methyl-3,4-dihydro-2H-isoquinolin-1-oneAusbeute 26 %

Reaktionsbedingungen

Temperatur
120 °C

Versuchsvorschrift

Under N2 protection, a mixture of [2-(3-chloro-phenyl)-1-methyl-ethyl]-carbamic acid methyl ester (1.2 g, 5.3 mmol) and PPA (polyphosphoric acid) (10 g) in a 100 mL round bottom flask was stirred at 120° C. for 2 hours. After cooling to room temperature, the reaction mixture was treated with ice-water and aqueous ammonia solution to adjust the pH to 8. The mixture was then extracted with ethyl acetate and the organic layer was washed with brine, dried over anhy. Na2SO4, filtered and concentrated in vacuo. The crude product obtained was further washed with ether to give 6-chloro-3-methyl-3,4-dihydro-2H-isoquinolin-1-one (0.27 g, 26%) (intermediate A-3-1) as a white solid. MS: 196.1 (M+H+). The ether filtrate was concentrated under reduced pressure and purified by flash chromatography to afford 8-chloro-3-methyl-3,4-dihydro-2H-isoquinolin-1-one (intermediate A-3-2) (54 mg, 5.2%) as a white solid. MS: 196.1 (M+H+).

Aufarbeitung

  1. temperatureAfter cooling to room temperature
  2. extractionThe mixture was then extracted with ethyl acetate
  3. washthe organic layer was washed with brine
  4. customdried over anhy
  5. filtrationNa2SO4, filtered
  6. concentrationconcentrated in vacuo
  7. customThe crude product obtained
  8. washwas further washed with ether

Quellen und Nachweise

ORD-Eintrag
ord-a77066daff1f4a99b8ec2e59a143ee0f
Quelldatensatz
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09133158B2

Notizen zur Reaktion

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