N,N-Dimethylglycine → 1-[5-[(Z)-2-cyano-2-(3,4-dimethoxy-phenyl)-vinyl]-thiophen-2-yl]-piperidin-4-yl dimethylamino-acetate

HRID 2366409Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2366409
[CH3:1][O:2][C:3]1[CH:4]=[C:5](/[C:11](=[CH:14]/[C:15]2[S:16][C:17]([N:20]3[CH2:25][CH2:24][CH:23]([OH:26])[CH2:22][CH2:21]3)=[CH:18][CH:19]=2)/[C:12]#[N:13])[CH:6]=[CH:7][C:8]=1[O:9][CH3:10].[CH3:27][N:28]([CH3:33])[CH2:29][C:30](O)=[O:31].C1(C)C=CC(S(Cl)(=O)=O)=CC=1>N1C=CC=CC=1>[CH3:27][N:28]([CH2:29][C:30]([O:26][CH:23]1[CH2:22][CH2:21][N:20]([C:17]2[S:16][C:15](/[CH:14]=[C:11](\[C:12]#[N:13])/[C:5]3[CH:6]=[CH:7][C:8]([O:9][CH3:10])=[C:3]([O:2][CH3:1])[CH:4]=3)=[CH:19][CH:18]=2)[CH2:25][CH2:24]1)=[O:31])[CH3:33]

Komponenten

5

Edukt 3

HCID 673N,N-DimethylglycineHCID 73974-Toluenesulfonyl chlorideHCID 16757522(Z)-2-(3,4-dimethoxyphenyl)-3-(5-(4-hydroxypiperidin-1-yl)thiophen-2-yl)acrylonitrile

Produkt 1

HCID 119656591-[5-[(Z)-2-cyano-2-(3,4-dimethoxy-phenyl)-vinyl]-thiophen-2-yl]-piperidin-4-yl dimethylamino-acetateAusbeute 76,5 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1049PyridineLösungsmittel

Versuchsvorschrift

Compound 6 (3.70 g) was dissolved in pyridine (100 mL), and N,N-dimethylglycin (5.15 g) was added to the solution, followed by stirring at room temperature for 1 hour. Subsequently, p-toluenesulfonyl chloride (9.43 g) was added to the mixture, followed by stirring under reflux for 12 hours. After completion of reaction, the solvent was evaporated to dryness. Chloroform (800 mL) was added to the residue, and the mixture was washed with water three times. The pH of the aqueous layer was checked by use of a pH testpaper, and adjusted to 4 to 5 with 1N aqueous hydrochloric acid. The organic layer was dried over sodium sulfate anhydrate, and the solvent was evaporated to dryness. The residue was purified by silica gel column chromatography (CHCl3-Hexane), to thereby yield the target product (yield: 3.48 g, 76%).

Aufarbeitung

  1. stirringby stirring
  2. temperatureunder reflux for 12 hours
  3. customAfter completion of reaction
  4. customthe solvent was evaporated to dryness
  5. additionChloroform (800 mL) was added to the residue
  6. washthe mixture was washed with water three times
  7. dry with materialThe organic layer was dried over sodium sulfate anhydrate
  8. customthe solvent was evaporated to dryness
  9. customThe residue was purified by silica gel column chromatography (CHCl3-Hexane)

Quellen und Nachweise

ORD-Eintrag
ord-811673dcd4ec46f58c50173a5a1a73e4
Quelldatensatz
uspto-grants-2014_04
Patentnummer
US08697742B2

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