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4-Methylbenzylamine → 6-Methylisoquinolin-3-amine

HRID 1875994
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1875994
C(O[CH:4](OCC)[C:5](=[NH:8])OC)C.[CH3:12][C:13]1[CH:14]=[CH:15][C:16]([CH2:19][NH2:20])=[CH:17][CH:18]=1>CO>[CH3:12][C:13]1[CH:14]=[C:15]2[C:4](=[CH:17][CH:18]=1)[CH:5]=[N:8][C:19]([NH2:20])=[CH:16]2
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 660354-MethylbenzylamineHCID 17874536Methyl 2,2-diethoxyethanecarboximidate

Produkt 1

HCID 187279006-Methylisoquinolin-3-amineAusbeute 63,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

To a solution of methyl 2,2-diethoxyacetimidate (1.1 g, 6.82 mmol) in methanol (8 mL) was added p-tolylmethanamine (0.788 g, 6.50 mmol) dropwise at ambient temperature. The reaction flask was then placed into a preheated oil-bath and stirred at 70° C. for 16 h, then removed and allowed cooled. The volatiles were removed under reduced pressure and the crude material was added dropwise to sulfuric acid (5 mL) at ambient temperature. The reaction mixture was stirred for 72 h, then the flask was placed into an ice-water bath, diluted with water (50 mL), and slowly neutralized to pH=10 with sodium hydroxide (10 N). As the reaction mixture became basic, a grey precipitate formed. This precipitate was filtered, washed with water, and dried to afford 6-methylisoquinolin-3-amine (0.65 g, 63%), as a grey powder. 1H NMR (400 MHz, DMSO-d6) δ ppm 8.73 (s, 1H), 7.69 (d, J=8.28 Hz, 1H), 7.29 (s, 1H), 7.00 (d, J=8.28 Hz, 1H), 5.81 (s, 1H), 2.40 (s, 3H). MS (LC/MS) R.T.=1.37; [M+H]+=159.10.

Aufarbeitung

  1. customThe reaction flask was then placed into a preheated oil-bath
  2. customremoved
  3. temperatureallowed cooled
  4. customThe volatiles were removed under reduced pressure
  5. additionthe crude material was added dropwise to sulfuric acid (5 mL) at ambient temperature
  6. stirringThe reaction mixture was stirred for 72 h
  7. customthe flask was placed into an ice-water bath
  8. additiondiluted with water (50 mL)
  9. customa grey precipitate formed
  10. filtrationThis precipitate was filtered
  11. washwashed with water
  12. customdried

Quellen und Nachweise

ORD-Eintrag
ord-28a5983c768b48529294153c78f9436a
Quelldatensatz
uspto-grants-2012_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08309577B2

Notizen zur Reaktion

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