Methanol → Methyl 2-(2-(2-chloro-5-fluorobenzylcarbamothioyl)hydrazono)propanoate

HRID 524123Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 524123
[C:1]([OH:6])(=[O:5])[C:2]([CH3:4])=O.[Cl:7][C:8]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:9]=1[CH2:10][NH:11][C:12]([NH:14][NH2:15])=[S:13].OS(O)(=O)=O.[CH3:26]O>>[Cl:7][C:8]1[CH:19]=[CH:18][C:17]([F:20])=[CH:16][C:9]=1[CH2:10][NH:11][C:12]([NH:14][N:15]=[C:2]([CH3:4])[C:1]([O:6][CH3:26])=[O:5])=[S:13]

Komponenten

5

Edukt 4

HCID 887MethanolHCID 1060Pyruvic AcidHCID 1118Sulfuric AcidHCID 86654854N-(2-chloro-5-fluorobenzyl)hydrazinecarbothioamide

Produkt 1

HCID 86654855Methyl 2-(2-(2-chloro-5-fluorobenzylcarbamothioyl)hydrazono)propanoate

Versuchsvorschrift

To a solution of pyruvic acid (5.63 g, 64.0 mmol) in methanol (150 mL) was added N-(2-chloro-5-fluorobenzyl)hydrazinecarbothioamide (27, 14.9 g, 64.0 mmol) followed by cone. H2SO4 (3 mL) The mixture was heated at reflux for 15 h. Most of the solvent was evaporated. The resulting residue was taken into EtOAc (500 mL), washed with water, saturated NaHCO3 and brine, dried over MgSO4, and concentrated to give methyl 2-(2-(2-chloro-5-fluorobenzylcarbamothioyl)hydrazono)propanoate (28). MS: m/z, 318 (100%, M+1), 320 (35%).

Aufarbeitung

  1. temperatureat reflux for 15 h
  2. customMost of the solvent was evaporated
  3. washwashed with water, saturated NaHCO3 and brine
  4. dry with materialdried over MgSO4
  5. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-5afd33211c30480ebbf11dc63f58766f
Quelldatensatz
uspto-grants-2016_05
Patentnummer
US09340523B2

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