Sodium Hydroxide → 4-{(1S)-1-[3-(3,5-dichlorophenyl)-5-(7-methoxyquinolin-3-yl)-1H-pyrazol-1-yl]ethyl}benzoic acid

HRID 1865427Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1865427
[Cl:1][C:2]1[CH:3]=[C:4]([C:9]2[CH:13]=[C:12]([C:14]3[CH:15]=[N:16][C:17]4[C:22]([CH:23]=3)=[CH:21][CH:20]=[C:19]([O:24][CH3:25])[CH:18]=4)[N:11]([C@H:26]([C:28]3[CH:38]=[CH:37][C:31]([C:32]([O:34]CC)=[O:33])=[CH:30][CH:29]=3)[CH3:27])[N:10]=2)[CH:5]=[C:6]([Cl:8])[CH:7]=1.[OH-].[Na+]>C1COCC1.CO>[Cl:8][C:6]1[CH:5]=[C:4]([C:9]2[CH:13]=[C:12]([C:14]3[CH:15]=[N:16][C:17]4[C:22]([CH:23]=3)=[CH:21][CH:20]=[C:19]([O:24][CH3:25])[CH:18]=4)[N:11]([C@H:26]([C:28]3[CH:29]=[CH:30][C:31]([C:32]([OH:34])=[O:33])=[CH:37][CH:38]=3)[CH3:27])[N:10]=2)[CH:3]=[C:2]([Cl:1])[CH:7]=1

Komponenten

4

Versuchsvorschrift

To a solution of the intermediate from step G (67 mg, 0.12 mmol) in 4 mL of 1:1 THF/MeOH was added sodium hydroxide (5N, 1 mL). After stirring the reaction at room temperature for 1 hour it was concentrated in vacuo to remove THF/MeOH. The resulting aqueous mixture was acidified with 1N HCl until the pH was slightly acidic (pH=5). The resulting solution was extracted with EtOAc (3×), and the combined organic layers were then washed with brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo. The resulting white solid was used without further purification.

Aufarbeitung

  1. customthe reaction at room temperature for 1 hour it
  2. concentrationwas concentrated in vacuo
  3. customto remove THF/MeOH
  4. extractionThe resulting solution was extracted with EtOAc (3×)
  5. washthe combined organic layers were then washed with brine
  6. dry with materialdried over anhydrous MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated in vacuo
  9. customThe resulting white solid was used without further purification

Quellen und Nachweise

ORD-Eintrag
ord-876a640a77d84311a4a1547abb02d276
Quelldatensatz
uspto-grants-2009_12
Patentnummer
US07625938B2

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