Triphenylphosphine → (S)-4-Benzyl-3-[(2S)-3-(4-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-2-methyl-phenyl)-2-ethoxy-propionyl]-oxazolidin-2-one

HRID 1064906

Reaktionsgleichung

Reaktionsgleichung von HRID 1064906
[CH2:1]([C@H:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:28])[C@@H:15]([O:25][CH2:26][CH3:27])[CH2:16][C:17]1[CH:22]=[CH:21][C:20]([OH:23])=[CH:19][C:18]=1[CH3:24])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[Cl:29][C:30]1[CH:35]=[CH:34][C:33]([C:36]2[O:37][C:38]([CH3:44])=[C:39]([CH2:41][CH2:42]O)[N:40]=2)=[CH:32][CH:31]=1.O=C(CC)CC(OC)=O.ClC1C=CC(C(N)=O)=CC=1.CC1OC(C2C=CC=CC=2)=NC=1CCO.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.N(C(OCC)=O)=NC(OCC)=O>O1CCCC1>[CH2:1]([C@H:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:28])[C@@H:15]([O:25][CH2:26][CH3:27])[CH2:16][C:17]1[CH:22]=[CH:21][C:20]([O:23][CH2:42][CH2:41][C:39]2[N:40]=[C:36]([C:33]3[CH:34]=[CH:35][C:30]([Cl:29])=[CH:31][CH:32]=3)[O:37][C:38]=2[CH3:44])=[CH:19][C:18]=1[CH3:24])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

9

Edukt 7

HCID 11776TriphenylphosphineHCID 120844-ChlorobenzamideHCID 121699Methyl 3-oxovalerateHCID 220568ethyl N-ethoxycarbonyliminocarbamateHCID 7255852-(5-Methyl-2-phenyl-4-oxazolyl)ethanolHCID 222739062-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanolHCID 68615907(S)-4-Benzyl-3-[(2S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionyl]-oxazolidin-2-one

Produkt 1

HCID 69282429(S)-4-Benzyl-3-[(2S)-3-(4-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-2-methyl-phenyl)-2-ethoxy-propionyl]-oxazolidin-2-oneAusbeute 46,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

To a ice cold solution of (S)-4-benzyl-3-[(2S)-2-ethoxy-3-(4-hydroxy-2-methyl-phenyl)-propionyl]-oxazolidin-2-one (100 mg, 260 μmol), 2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol (93 mg, 390 μmol) (prepared from methyl 3-oxopentanoate and 4-chloro-benzamide in analogy to the sequence described for the synthesis of 2-(5-methyl-2-phenyl-oxazol-4-yl)-ethanol in M. Scalone, PCT WO 01/79202 A1) and triphenylphosphine (103 mg, 390 μmol) in tetrahydrofuran (2.5 ml) was added diethyl azodicarboxylate (61 μl, 390 μmol). The cooling bath was removed and stirring was continued for 12 h. Evaporation of the solvent under reduced pressure gave a yellow oil which was purified by column chromatography (silica gel, cyclohexane/AcOEt) to give 70 mg (120 μmol, 45%) of the title compound as colorless oil.

Aufarbeitung

  1. customThe cooling bath was removed
  2. customEvaporation of the solvent under reduced pressure
  3. customgave a yellow oil which
  4. customwas purified by column chromatography (silica gel, cyclohexane/AcOEt)

Quellen und Nachweise

ORD-Eintrag
ord-4d776061f2fc469cba6d3039a012ce61
Quelldatensatz
uspto-grants-2005_11
Patentnummer
US06969725B2

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