Acetic Acid → (R)-4-chloro-8-oxo-9-(2,2,2-trifluoroethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl benzoate

HRID 132446Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 132446
[C:1]([O:9][C@H:10]([CH2:15][C:16]1[C:17]([CH2:26][NH:27][CH2:28][C:29]([F:32])([F:31])[F:30])=[C:18]2[C:22](=[C:23]([Cl:25])[CH:24]=1)[NH:21][N:20]=[CH:19]2)[C:11]([O:13]C)=O)(=[O:8])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C1(C)C=CC=CC=1.C(O)(=O)C>>[C:1]([O:9][C@H:10]1[C:11](=[O:13])[N:27]([CH2:28][C:29]([F:31])([F:32])[F:30])[CH2:26][C:17]2[C:18]3[CH:19]=[N:20][NH:21][C:22]=3[C:23]([Cl:25])=[CH:24][C:16]=2[CH2:15]1)(=[O:8])[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1

Komponenten

4

Versuchsvorschrift

(R)-3-(7-chloro-4-((2,2,2-trifluoroethylamino)methyl)-1H-indazol-5-yl)-1-methoxy-1-oxopropan-2-yl benzoate (7.75 g, 16.5 mmol) in toluene (70.00 ml, 657 mmol) was added acetic acid (1.2 ml, 20.96 mmol) and refluxed for 12 h. The solvent was evaporated and the crude product was dissolved in EtOAc, washed with aqueous NaHCO3. The solvent was removed and the crude product was purified by flash chromatography using 50% EtOAc in hexane to give (R)-4-chloro-8-oxo-9-(2,2,2-trifluoroethyl)-3,6,7,8,9,10-hexahydroazepino[3,4-e]indazol-7-yl benzoate in 74% yield. MS (ESI) 438 (M+H); Rf=2.60.

Aufarbeitung

  1. temperaturerefluxed for 12 h
  2. customThe solvent was evaporated
  3. dissolutionthe crude product was dissolved in EtOAc
  4. washwashed with aqueous NaHCO3
  5. customThe solvent was removed
  6. customthe crude product was purified by flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-44b458d788c347e996dcb59c412ba105
Quelldatensatz
uspto-grants-2008_06
Patentnummer
US07384931B2

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