Reaktion #167400

ord-80d35979a62f4716a784efb136d58677

Reaktionsgleichung

CO
methanol
C=C(C)C(=O)O
2-Methyl-acrylic acid
Oc1ccc(O)cc1
Benzene-1,4-diol
Nc1ccc2ncsc2c1
Benzothiazol-6-ylamine
CC(CNc1ccc2ncsc2c1)C(=O)O
product
Ausbeute 27.4%
CC(CNc1ccc2ncsc2c1)C(=O)O
3-(Benzothiazol-6-ylamino)-2-methyl-propionic Acid
Ausbeute 27.4%

Lösungsmittel

Reaktionsbedingungen

Temperatur
100°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe resulting reaction mass
  2. 2
    TemperaturThe reaction mixture was cooled to room temperature
  3. 3
    Sonstigepartitioned between water and ethyl acetate
  4. 4
    WaschenThe organic layer was washed with brine solution
  5. 5
    Trocknendried over Na2SO4
  6. 6
    Einengenconcentrated
  7. 7
    Sonstigeto afford the crude product
  8. 8
    SonstigePurification by column chromatography on silica gel (0.75% methanol in chloroform)

Vorschrift

2-Methyl-acrylic acid (0.63 g, 0.00732 mol) and Benzene-1,4-diol (0.029 g, 0.000266 mol) were added to a stirred solution of Benzothiazol-6-ylamine (1 g, 0.00665 mol) in toluene (6 mL) under nitrogen atmosphere. The resulting reaction mass was heated at 70° C. for 72 hours and further at 100° C. for 48 hours. The reaction was monitored by TLC (5% methanol in chloroform). The reaction mixture was cooled to room temperature and partitioned between water and ethyl acetate. The organic layer was washed with brine solution, dried over Na2SO4 and concentrated to afford the crude product. Purification by column chromatography on silica gel (0.75% methanol in chloroform) afforded 0.43 g of the product (26.87% yield).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE045173E1uspto-grants-2014_09