Water → HCID 19360267, Verbindung

HRID 1728619Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1728619
[NH2:1][C:2]1[C:3]2[CH:10]=[CH:9][C:8]([Cl:11])=[CH:7][C:4]=2[S:5][CH:6]=1.Cl.Cl[C:14]1[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=1.O>CN1CCCC1=O>[ClH:11].[Cl:11][C:8]1[CH:9]=[CH:10][C:3]2[C:2]([NH:1][C:14]3[CH:19]=[CH:18][N:17]=[CH:16][CH:15]=3)=[CH:6][S:5][C:4]=2[CH:7]=1

Komponenten

5

Edukt 3

HCID 962WaterHCID 818524-Chloropyridine hydrochlorideHCID 193602466-Chlorobenzo[b]thiophen-3-amine

Produkt 1

HCID 19360267HCID 19360267, VerbindungAusbeute 174,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 13387N-methyl-2-pyrrolidoneLösungsmittel

Versuchsvorschrift

A solution of 3-amino-6-chlorobenzo[b]thiophene (5 g, 27 mmol) and 4-chloropyridine hydrochloride (6 g, 40 mmol) in 75 mL of 1-methyl-2-pyrrolidinone was stirred at 80° for 1.5 h, and then was cooled, stirred with water and extracted with ether. The aqueous layer was basified with sodium carbonate and extracted with ethyl acetate. The organic extract was washed with water and saturated sodium chloride solution and then was dried (anhydrous magnesium sulfate), filtered and concentrated to a dark oil. Elution through silica with ethyl acetate via flash column chromatography yielded 7 g of an amber oil. Conversion to the hydrochloride salt in 20% methanol in ether yielded 4.2 g of yellow crystals, mp 264°-266° (dec.).

Aufarbeitung

  1. temperaturewas cooled
  2. extractionextracted with ether
  3. extractionextracted with ethyl acetate
  4. extractionThe organic extract
  5. washwas washed with water and saturated sodium chloride solution
  6. dry with materialwas dried (anhydrous magnesium sulfate)
  7. filtrationfiltered
  8. concentrationconcentrated to a dark oil
  9. washElution through silica with ethyl acetate via flash column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-b24312be623d458fba6ab1ecb7ade5e8
Quelldatensatz
uspto-grants-1994_07
Patentnummer
US05328920

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