Pyridine → 2-n-Propylamino-5-n-propyl thiazole-4-carboxylic acid ethyl ester

HRID 2256202Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2256202
[CH2:1]([NH:4][C:5]([NH2:7])=[S:6])[CH2:2][CH3:3].[CH2:8]([O:10][C:11](=[O:19])[C:12](=O)[CH:13](Cl)[CH2:14][CH2:15][CH3:16])[CH3:9].N1C=CC=CC=1>C(O)C>[CH2:8]([O:10][C:11]([C:12]1[N:7]=[C:5]([NH:4][CH2:1][CH2:2][CH3:3])[S:6][C:13]=1[CH2:14][CH2:15][CH3:16])=[O:19])[CH3:9]

Komponenten

5

Edukt 3

HCID 1049PyridineHCID 1615208Propyl-2-thioureaHCID 11030654Ethyl 3-chloro-2-oxohexanoate

Produkt 1

HCID 540564382-n-Propylamino-5-n-propyl thiazole-4-carboxylic acid ethyl esterAusbeute 68,3 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 702EthanolLösungsmittel

Versuchsvorschrift

n-Propylthiourea (270 mg), 3-chloro-2-oxohexanoic acid ethyl ester (441 mg), and pyridine (0.28 ml) were added to ethanol (10 ml), and the solution was refluxed for 3.5 hours. The solvent was evaporated. The residue was extracted with chloroform (20 ml), and washed with dilute hydrochloric acid solution (10 ml). The organic layer was dried over anhydrous magnesium sulfate and evaporated. The residue was purified by column chromatography on silica gel (eluent:chloroform/methanol=100/1), 2-n-propylamino-5-n-propyl thiazole-4-carboxylic acid ethyl ester (400 mg) was obtained.

Aufarbeitung

  1. temperaturethe solution was refluxed for 3.5 hours
  2. customThe solvent was evaporated
  3. extractionThe residue was extracted with chloroform (20 ml)
  4. washwashed with dilute hydrochloric acid solution (10 ml)
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. customevaporated
  7. customThe residue was purified by column chromatography on silica gel (eluent:chloroform/methanol=100/1)

Quellen und Nachweise

ORD-Eintrag
ord-522bb2c0464e4c898072f6b233d9a168
Quelldatensatz
uspto-grants-1997_08
Patentnummer
US05654322

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