Water → HCID 178448116, Verbindung

HRID 747851Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 747851
[CH:1]([C@H:4]1[CH2:9][CH2:8][C@H:7]([NH:10][C:11]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[C:14]([CH2:21][C:22]3[CH:27]=[CH:26][N:25]=[C:24]([O:28]C)[CH:23]=3)=[N:13][N:12]=2)[CH2:6][CH2:5]1)([CH3:3])[CH3:2].C([O-])(O)=O.[Na+].O.CCOC(C)=O>C(Cl)(Cl)Cl.CO>[CH:1]([C@H:4]1[CH2:5][CH2:6][C@H:7]([NH:10][C:11]2[C:20]3[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=3)[C:14]([CH2:21][C:22]3[CH:27]=[CH:26][N:25]=[C:24]([OH:28])[CH:23]=3)=[N:13][N:12]=2)[CH2:8][CH2:9]1)([CH3:3])[CH3:2]

Komponenten

7

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

Under N2-atmosphere, 0.28 ml (2.05 mMol) Me3Sil are added to 400 mg (1.02 mMol) of trans 1-(4-isopropyl-cyclohexylamino)-4-[2-methoxy-(pyridin-4-yl)-methyl]-phthalazine in 10 ml chloroform, and the resulting mixture is stirred during 20 h at 60° C. After cooling to RT, 5 ml sat. NaHCO3-solution, 5 ml water, 20 ml EtOAc and a small amount of methanol are added, followed by agitation. The resulting white crystals are filtered off, washed with water and dried, yielding the title compound: M.p. 266-267° C. (decomposition); FAB-MS: (M+H)+=377; HPLC(Grad20-100) tRet=10.3). From the filtrate, by extraction with EtOAc, washing of the organic phase with water and brine, drying (Na2SO4), evaporation and crystallisation from dichlormethane/methanol under addition of ether, more product results.

Aufarbeitung

  1. temperatureAfter cooling to RT
  2. filtrationThe resulting white crystals are filtered off
  3. washwashed with water
  4. customdried

Quellen und Nachweise

ORD-Eintrag
ord-8c8d8b14f5844a18973a82f8ce9001d6
Quelldatensatz
uspto-grants-2008_07
Patentnummer
US07399761B2

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