Diisopropylethylamine → Methyl 2-amino-3-[(methoxyacetyl)amino]benzoate

HRID 1505769Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1505769
[NH2:1][C:2]1[C:11]([NH2:12])=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5].C(N(CC)C(C)C)(C)C.[CH3:22][O:23][CH2:24][C:25](Cl)=[O:26].C(=O)(O)[O-].[Na+]>C1COCC1>[NH2:1][C:2]1[C:11]([NH:12][C:25](=[O:26])[CH2:24][O:23][CH3:22])=[CH:10][CH:9]=[CH:8][C:3]=1[C:4]([O:6][CH3:7])=[O:5]

Komponenten

6

Versuchsvorschrift

To a solution of methyl 2,3-diaminobenzoate (3.0 g) in THF (50 mL) was added N,N-diisopropylethylamine (4.0 mL). The solution was stirred under ice-cooling, methoxyacetyl chloride (1.81 mL) in THF (10 mL) was added dropwise slowly, and it was stirred for 3 hours at the same temperature. To the reaction mixture was added saturated aqueous sodium bicarbonate, and THF was removed under reduced pressure. To the residue was added saturated aqueous sodium bicarbonate, and it was extracted with ethyl acetate, dried over anhydrous magnesium sulfate, and the solvent was removed under reduced pressure. The residue was purified on silica gel column chromatography to obtain the titled compound (3.60 g) as pale yellow powder.

Aufarbeitung

  1. temperaturecooling
  2. stirringit was stirred for 3 hours at the same temperature
  3. customwas removed under reduced pressure
  4. additionTo the residue was added saturated aqueous sodium bicarbonate, and it
  5. extractionwas extracted with ethyl acetate
  6. dry with materialdried over anhydrous magnesium sulfate
  7. customthe solvent was removed under reduced pressure
  8. customThe residue was purified on silica gel column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-1e057f0fd1ca46ac82da946409a3220a
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09216968B2

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