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2-Methyl-2-thiopseudourea sulfate → HCID 54014435, Verbindung

HRID 650632
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 650632
C([O-])(=O)C.[Na+].S(O)(O)(=O)=O.[CH3:11][S:12][C:13](=[NH:15])[NH2:14].[CH2:16]([O:18][C:19](=[O:34])[C:20]([C:25](=O)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=1[Br:32])=[CH:21]N(C)C)[CH3:17]>CN(C)C=O>[CH2:16]([O:18][C:19]([C:20]1[C:25]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=2[Br:32])=[N:15][C:13]([S:12][CH3:11])=[N:14][CH:21]=1)=[O:34])[CH3:17]
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Komponenten

5

Edukt 3

HCID 752702-Methyl-2-thiopseudourea sulfateHCID 517045Sodium AcetateHCID 541240112-(2-Bromo-benzoyl)-3-dimethylamino-acrylic acid ethyl ester

Produkt 1

HCID 54014435HCID 54014435, VerbindungAusbeute 69,6 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel2×

Versuchsvorschrift

To a suspension of 3.81 g (46.54 mmol) sodiumacetate and 6.47 g (23.27 mmol) S-methylisothiourea sulfate in 100 ml N,N-dimethylformamide a solution of 6.90 g (21.15 mmol) 2-(2-bromo-benzoyl)-3-dimethylamino-acrylic acid ethyl ester in 20 ml N,N-dimethylformamide was added at once and the resulting reaction mixture was stirred for 16 hrs. at 90°. The solvent was evaporated and the residue distributed between 100 ml CH2Cl2 and 100 ml H2O. The aqueous phase was extracted twice with 100 ml CH2Cl2. The combined organic layers were dried (MgSO4), filtered and evaporated. The residue was purified by chromatography (SiO2, CH2Cl2) to give 5.20 g (69%) 4-(2-bromo-phenyl)-2-methylsulfanyl-pyrimidine-5-carboxylic acid ethyl ester as a pale green oil.

Aufarbeitung

  1. additionwas added at once and
  2. customthe resulting reaction mixture
  3. customat 90°
  4. customThe solvent was evaporated
  5. extractionThe aqueous phase was extracted twice with 100 ml CH2Cl2
  6. dry with materialThe combined organic layers were dried (MgSO4)
  7. filtrationfiltered
  8. customevaporated
  9. customThe residue was purified by chromatography (SiO2, CH2Cl2)

Quellen und Nachweise

ORD-Eintrag
ord-fdecb561c2d74f8985e8bcdfea01981e
Quelldatensatz
uspto-grants-2001_08
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06274588B1

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