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Methyl iodide → 7-Bromo-2-methyl-1,6-naphthyridine

HRID 523077
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 523077
[NH2:1][C:2]1[CH:7]=[C:6]([Br:8])[N:5]=[CH:4][C:3]=1/[CH:9]=[CH:10]/[C:11](=O)[CH3:12].C[S-].[Na+].IC>C(O)C>[Br:8][C:6]1[CH:7]=[C:2]2[C:3]([CH:9]=[CH:10][C:11]([CH3:12])=[N:1]2)=[CH:4][N:5]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 6328Methyl iodideHCID 4378561Sodium methanethiolateHCID 89995621(E)-4-(4-Amino-6-bromopyridin-3-yl)but-3-en-2-one

Produkt 1

HCID 899956197-Bromo-2-methyl-1,6-naphthyridineAusbeute 90 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

(E)-4-(4-Amino-6-bromopyridin-3-yl)but-3-en-2-one (Preparation 66, 331 mg 1.37 mmol) and sodium thiomethoxide (97.5 mg 1.39 mmol) were stirred in ethanol (2.9 mL) at 20° C. for 50 minutes. Iodomethane (86 uL, 1.38 mmole) was added and the reaction stirred for another 45 minutes. The reaction was concentrated in vacuo and diluted with ethyl acetate (30 mL) and washed with water (10 mL). The aqueous was back extracted with ethyl acetate (5 mL) and the combined organic layers were washed with brine, dried over sodium sulfate and concentrated in vacuo to afford the title compound (275 mg, 89%).

Aufarbeitung

  1. concentrationThe reaction was concentrated in vacuo
  2. additiondiluted with ethyl acetate (30 mL)
  3. washwashed with water (10 mL)
  4. extractionThe aqueous was back extracted with ethyl acetate (5 mL)
  5. washthe combined organic layers were washed with brine
  6. dry with materialdried over sodium sulfate
  7. concentrationconcentrated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-77f27829e73446deb99cc615115187ac
Quelldatensatz
uspto-grants-2016_05
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09334286B2

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