Triphenylphosphine → HCID 86643670, Verbindung

HRID 215855Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 215855
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.C(OC(=O)O[C@H:25]1[CH2:29][C@@H:28]([N:30]2[CH:38]=[N:37][C:36]3[C:31]2=[N:32][C:33]([Cl:40])=[N:34][C:35]=3[Cl:39])[CH:27]=[CH:26]1)C.[CH2:42]([C:44]1[CH:48]=[N:47][NH:46][N:45]=1)[CH3:43]>C1COCC1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.C1C=CC(/C=C/C(/C=C/C2C=CC=CC=2)=O)=CC=1.[Pd].[Pd]>[Cl:40][C:33]1[N:32]=[C:31]2[C:36]([N:37]=[CH:38][N:30]2[C@@H:28]2[CH2:29][C@H:25]([N:47]3[CH:48]=[C:44]([CH2:42][CH3:43])[N:45]=[N:46]3)[CH:26]=[CH:27]2)=[C:35]([Cl:39])[N:34]=1

Komponenten

6

Versuchsvorschrift

A mixture comprising triphenylphosphine (0.299 g, 0.874 mmol) and Pd2(dba)3 (0.267 g, 0.291 mmol) in dry THF (5 mL) under an inert atmosphere of argon is stirred at RT for 10 minutes. This mixture is then added to a pre-stirring mixture of carbonic acid (1S,4R)-4-(2,6-dichloro-purin-9-yl)-cyclopent-2-enyl ester ethyl ester (Intermediate AA2) (2.00 g, 5.83 mmol) and 4-ethyl-2H-[1,2,3]triazole (0.594 g, 6.12 mmol) in THF (15 mL). The resulting mixture is stirred at RT overnight and then concentrated in vacuo. The crude product is purified by chromatography on silica eluting with 0-50% EtOAc in iso-hexane to afford the title compound as a white solid. (MH+ 350).

Aufarbeitung

  1. concentrationconcentrated in vacuo
  2. customThe crude product is purified by chromatography on silica eluting with 0-50% EtOAc in iso-hexane

Quellen und Nachweise

ORD-Eintrag
ord-1d4ea045696d4bc38530429a916155ad
Quelldatensatz
uspto-grants-2012_06
Patentnummer
US08193164B2

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