1-Methylimidazole → (S)-N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide

HRID 424881

Reaktionsgleichung

Reaktionsgleichung von HRID 424881
[C:1]([CH2:9][CH2:10][C:11]([OH:13])=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CN1C=CN=C1.C1(C)C=CC(S(Cl)(=O)=O)=CC=1.[CH2:31]([C:33]1[N:34]=[C:35]([C@@H:38]([NH2:49])[CH2:39][C:40]2[CH:45]=[CH:44][C:43]([N+:46]([O-:48])=[O:47])=[CH:42][CH:41]=2)[S:36][CH:37]=1)[CH3:32]>C(Cl)Cl>[CH2:31]([C:33]1[N:34]=[C:35]([C@@H:38]([NH:49][C:11](=[O:13])[CH2:10][CH2:9][C:1](=[O:8])[C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH2:39][C:40]2[CH:45]=[CH:44][C:43]([N+:46]([O-:48])=[O:47])=[CH:42][CH:41]=2)[S:36][CH:37]=1)[CH3:32]

Komponenten

6

Versuchsvorschrift

3-Benzoylpropionic acid (0.250 g) is dissolved in CH2Cl2 (5 mL), N-methyl imidazole (0.333 mL) is added and the resulting solution is cooled to 0° C. after which a solution of p-toluenesulfonyl chloride (0.320 g) in CH2Cl2 (2 mL) is added dropwise. After 0.5 hours (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine, 3, (0.388 g) is added. The reaction is stirred for 18 hours at room temperature and then concentrated in vacuo. The resulting residue is dissolved in EtOAc and washed with 1N HCl and brine. The solution is dried over Na2SO4, filtered, and concentrated and the crude material purified over silica to afford 0.415 g of the desired product.

Aufarbeitung

  1. additionis added dropwise
  2. concentrationconcentrated in vacuo
  3. dissolutionThe resulting residue is dissolved in EtOAc
  4. washwashed with 1N HCl and brine
  5. dry with materialThe solution is dried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customthe crude material purified over silica

Quellen und Nachweise

ORD-Eintrag
ord-6b0e7d0dd83147b2a4c466ddbd9eada2
Quelldatensatz
uspto-grants-2012_01
Patentnummer
US08106078B2

Verknüpfte Notizen

Wird geladen…