Hydrochloric Acid → Methyl 3-(5-methyl-2-thienylamino)-4-oxopentanoate

HRID 1597457Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1597457
C[C:2]1[S:6][C:5]([C:7](O)=O)=[CH:4][CH:3]=1.S(Cl)(Cl)=O.Cl.CC(C(O)=O)[C@@H:17]([C:19]([OH:21])=O)[NH2:18].[C:25]([O:28][C:29](=[O:31])[CH3:30])(=O)C.Cl.[C:33]1(C)C=CC=CC=1>N1C=CC=CC=1>[CH3:7][C:5]1[S:6][C:2]([NH:18][CH:17]([C:19](=[O:21])[CH3:33])[CH2:30][C:29]([O:28][CH3:25])=[O:31])=[CH:3][CH:4]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
70 °C

Versuchsvorschrift

A slurry of 19.3 g (0.136 mol) 5-methyl-2-thiophenecarboxylic acid in 200 mL of toluene was treated with 10.9 mL (0.15 mol) of thionyl chloride. The resulting mixture was heated to 70° C. for 16 h, then concentrated in vacuo. The resulting oil was added in portions to a solution of 25.0 g (0.136 mol) of b-methylaspartic acid hydrochloride in 80 mL of pyridine at 0° C. at a rate to maintain a temperature <10° C. After the addition was complete the solution was allowed to stir at 25° C. for 1 h, treated with 50 mL of acetic anhydride and heated to 90° C. for 2 h. The mixture was then cooled to 25° C., poured into 700 mL of 1N HCl, and extracted three times with EtOAc. The combined organic phases were washed three times with 3 N HCl, once with water, once with 5% Aq NaHCO3, and finally with brine. The solution was dried (Na2SO4), then chromatographed over silica gel eluting with hexanes:EtOAc 3//2 to obtain 9.1 g (25%) of the title compound as a clear yellow oil: MS (ES+) m/e 270 (MH+).

Aufarbeitung

  1. concentrationconcentrated in vacuo
  2. temperatureto maintain a temperature <10° C
  3. additionAfter the addition
  4. temperatureheated to 90° C. for 2 h
  5. temperatureThe mixture was then cooled to 25° C.
  6. extractionextracted three times with EtOAc
  7. washThe combined organic phases were washed three times with 3 N HCl
  8. dry with materialThe solution was dried (Na2SO4)
  9. customchromatographed over silica gel eluting with hexanes

Quellen und Nachweise

ORD-Eintrag
ord-bd8afa5cdc1549baa04a5d1d2a025d71
Quelldatensatz
uspto-grants-2001_09
Patentnummer
US06294580B1

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