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Dimethylformamide → 3-methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-one

HRID 33963
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 33963
C(O[C:4](=[O:16])[CH2:5][C:6]1[CH:15]=[CH:14][C:13]2[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=2)[CH:7]=1)C.[C:17]([C:19]1[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=1)#[N:18].CC(C)([O-])C.[K+].[CH3:31][S:32]N=C=O.IC.[CH3:38][N:39]([CH3:42])C=O>>[CH3:38][N:39]1[C:4](=[O:16])[C:5]([C:6]2[CH:15]=[CH:14][C:13]3[C:8](=[CH:9][CH:10]=[CH:11][CH:12]=3)[CH:7]=2)=[C:17]([C:19]2[CH:24]=[CH:23][N:22]=[CH:21][CH:20]=2)[N:18]=[C:42]1[S:32][CH3:31]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 6

HCID 6228Dimethylformamide2×HCID 6328Methyl iodideHCID 75064-CyanopyridineHCID 256821Ethyl 2-naphthylacetateHCID 21933440MethylthioisocyanateHCID 23665647Potassium tert-butoxide

Produkt 1

HCID 22346641
3-methyl-2-methylsulfanyl-5-naphthalen-2-yl-6-pyridin-4-yl-3H-pyrimidin-4-one

Versuchsvorschrift

To a stirring solution of ethyl-2-naphthylacetate (10.0 g, 46.7 mmol) and 4-cyanopyridine (4.86 g, 46.7 mmol) in 50 mL dry dimethylformamide (DMF) at room temperature under nitrogen was added 47 mL potassium tert-butoxide (1.0 M in 2-methyl-2-propanol) dropwise via syringe. The dark red solution was stirred at room temperature for 75 min. Methylthioisocyanate (3.41 g, 46.7 mmol) in 10 mL DMF added whole. The solution was stirred for 90 min at room temperature. Iodomethane (2.95 mL, 46.7 mmol) was added dropwise over a 3 min period. Solid precipitates out of reaction. Continued to stir as a mixture for 30 min. Water (500 mL) was slowly added to reaction mixture. The solid was collected via filtration then washed with water, cold ethanol (50 mL), and ether. The solid was air dried for 3 days. M+1=360.2.

Aufarbeitung

  1. stirringThe solution was stirred for 90 min at room temperature
  2. customSolid precipitates out of reaction
  3. stirringto stir as a mixture for 30 min
  4. additionWater (500 mL) was slowly added to reaction mixture
  5. filtrationThe solid was collected via filtration
  6. washthen washed with water, cold ethanol (50 mL), and ether
  7. customdried for 3 days

Quellen und Nachweise

ORD-Eintrag
ord-77270c2e721440a28b95e897fee0bb01
Quelldatensatz
uspto-grants-2008_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07429594B2

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