Sodium hydride → 2-chloro-N-(isoxazol-3-yl)methyl-N-(2,6-dimethylphenyl)acetamide

HRID 27337

Reaktionsgleichung

Reaktionsgleichung von HRID 27337
[Cl:1][CH2:2][C:3]([NH:5][C:6]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][C:7]=1[CH3:13])=[O:4].Br[CH2:15][C:16]1[CH:20]=[CH:19][O:18][N:17]=1.[H-].[Na+]>CN(C)C=O>[Cl:1][CH2:2][C:3]([N:5]([CH2:15][C:16]1[CH:20]=[CH:19][O:18][N:17]=1)[C:6]1[C:11]([CH3:12])=[CH:10][CH:9]=[CH:8][C:7]=1[CH3:13])=[O:4]

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 707982-Chloro-N-(2,6-dimethylphenyl)acetamideHCID 104646163-(Bromomethyl)-1,2-oxazole

Produkt 1

HCID 130376022-chloro-N-(isoxazol-3-yl)methyl-N-(2,6-dimethylphenyl)acetamide

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

A mixture of 6.1 g N-chloroacetyl-2,6-dimethylaniline and 5 g 3-bromomethylisoxazole (prepared as in Example 6 above) in 200 ml dry dimethylformamide was treated with 1.5 g sodium hydride as in Example 3 above. After workup, the solid product was purified by column and high-pressure liquid chromatography to yield a pure product, m.p. 78°-81° C. This product is shown as Compound 2 in Table I. C14H15ClN2O2 : calc., %C 60.32, %H 5.39, %N 10.05; found, %C 60.72, %H 5.71, %N 8.85.

Aufarbeitung

  1. customAfter workup, the solid product was purified by column and high-pressure liquid chromatography
  2. customto yield a pure product, m.p. 78°-81° C

Quellen und Nachweise

ORD-Eintrag
ord-865d1a1ecb8f4ee79b385fa61a1a521e
Quelldatensatz
uspto-grants-1980_09
Patentnummer
US04221584

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