Reaktion #95683

ord-39334f19e71744d793e29b729d245f50

Reaktionsgleichung

COc1ccc(CNCC(=O)O)c(OC)c1
N-(2,4-dimethoxybenzyl)-glycine
[Cl-].[Na+]
sodium chloride
O=c1[nH]c2ccccc2c(=O)o1
isatoic acid anhydride
NCC(=O)O
glycine
COc1ccc(C=O)c(OC)c1
2,4-dimethoxybenzaldehyde
[Na+].[OH-]
sodium hydroxide
Cl
hydrochloric acid
COc1ccc(CNCC(=O)O)c(OC)c1
N-(2,4-dimethoxybenzyl)glycine
COc1ccc(CN2CC(=O)Nc3ccccc3C2=O)c(OC)c1
3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dione

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    SonstigeThe aqueous solution obtained
  2. 2
    Einengenis concentrated
  3. 3
    FiltrationThe separated crystals are filtered off under suction
  4. 4
    Waschenwashed with water
  5. 5
    Sonstigedried
  6. 6
    SonstigeAfter recrystallisation from ethyl acetate

Vorschrift

N-(2,4-dimethoxybenzyl)glycine is prepared by the reaction of glycine with 2,4-dimethoxybenzaldehyde in the presence of sodium hydroxide, reduction with palladium-on-carbon in methanol and subsequent neutralisation with 2 N hydrochloric acid. The aqueous solution obtained is concentrated. 41.9 g of this mixture of N-(2,4-dimethoxybenzyl)-glycine and sodium chloride are stirred at 110° C. for 1.5 hours in 300 ml of dimethyl sulphoxide with 23.18 g (142 mmol) of isatoic acid anhydride. The mixture is poured into ca 2 liters of water and stirred for 0.5 hour. The separated crystals are filtered off under suction, washed with water and dried. After recrystallisation from ethyl acetate, there is obtained 3,4-dihydro-4-(2,4-dimethoxybenzyl)-2H-1,4-benzodiazepine-2,5(1H)-dione of melting point 151°-152.5° C.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US04346032uspto-grants-1982_08