p-Toluenesulfonic acid → (R)-3-phenyl-2-(5-phenyl-benzoxazol-2-ylmethoxycarbonylamino) Propionic Acid Allyl Ester

HRID 2120603Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2120603
[C:1]1([C:7]2[CH:8]=[CH:9][C:10]3[O:14][C:13]([CH2:15][OH:16])=[N:12][C:11]=3[CH:17]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[C:18](N1C=CN=C1)(N1C=CN=C1)=[O:19].CC1C=CC(S(O)(=O)=O)=CC=1.[CH2:41]([O:44][C:45](=[O:55])[C@@H:46]([CH2:48][C:49]1[CH:54]=[CH:53][CH:52]=[CH:51][CH:50]=1)[NH2:47])[CH:42]=[CH2:43].C(N(CC)CC)C>C(Cl)Cl>[CH2:41]([O:44][C:45](=[O:55])[C@H:46]([NH:47][C:18]([O:16][CH2:15][C:13]1[O:14][C:10]2[CH:9]=[CH:8][C:7]([C:1]3[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=3)=[CH:17][C:11]=2[N:12]=1)=[O:19])[CH2:48][C:49]1[CH:50]=[CH:51][CH:52]=[CH:53][CH:54]=1)[CH:42]=[CH2:43]

Komponenten

7

Versuchsvorschrift

(5-Phenyl-benzoxazole-2-yl)methanol 51 (437 mg, 1.94 mmol) and carbonyldiimidazole (393 mg, 2.43 mmol) in 7 ml of dry CH2Cl2 were stirred at room temperature for 3 hrs. The tosic acid salt of (R)-phenylalanine allyl ester(767 mg, 1.94 mmol) was added followed by 0.42 ml of triethylamine (301 mg, 2.98 mmol). The mixture was stirred overnight. The mixture was diluted and washed with 1M HCl solution then with brine. After drying, the organic phase was filtered and concentrated. The crude product was chromatographed to give about 711 mg of (R)-3-phenyl-2-(5-phenyl-benzoxazol-2-ylmethoxycarbonylamino) propionic acid allyl ester 52.

Aufarbeitung

  1. additionThe mixture was diluted
  2. washwashed with 1M HCl solution
  3. customAfter drying
  4. filtrationthe organic phase was filtered
  5. concentrationconcentrated
  6. customThe crude product was chromatographed

Quellen und Nachweise

ORD-Eintrag
ord-36fc440f2b8440c2a93eaabac0d6390e
Quelldatensatz
uspto-grants-2004_02
Patentnummer
US06693098B2

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