Lithium Hydroxide → [4-(4'-Trifluoromethylbiphenyl-2-carbonyl-amino)piperidin-1-yl]acetic acid

HRID 1864969Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1864969
C([O:3][C:4](=[O:31])[CH2:5][N:6]1[CH2:11][CH2:10][CH:9]([NH:12][C:13]([C:15]2[C:16]([C:21]3[CH:26]=[CH:25][C:24]([C:27]([F:30])([F:29])[F:28])=[CH:23][CH:22]=3)=[CH:17][CH:18]=[CH:19][CH:20]=2)=[O:14])[CH2:8][CH2:7]1)C.[OH-].[Li+]>O1CCCC1CO>[F:30][C:27]([F:28])([F:29])[C:24]1[CH:25]=[CH:26][C:21]([C:16]2[C:15]([C:13]([NH:12][CH:9]3[CH2:8][CH2:7][N:6]([CH2:5][C:4]([OH:31])=[O:3])[CH2:11][CH2:10]3)=[O:14])=[CH:20][CH:19]=[CH:18][CH:17]=2)=[CH:22][CH:23]=1

Komponenten

4

Edukt 2

HCID 3939Lithium HydroxideHCID 57683250[4-(4'-Trifluoromethylbiphenyl-2-carbonylamino)piperidin-1-yl]acetic acid ethyl ester

Produkt 1

HCID 23033209[4-(4'-Trifluoromethylbiphenyl-2-carbonyl-amino)piperidin-1-yl]acetic acidAusbeute 73,8 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 7360Tetrahydrofurfuryl alcoholLösungsmittel

Versuchsvorschrift

To a solution of [4-(4′-trifluoromethylbiphenyl-2-carbonylamino)piperidin-1-yl]acetic acid ethyl ester (595 mg) obtained in Example 8c) in tetrahydrofuran-methanol (1:2; 10.2 mL) was added 1M aqueous lithium hydroxide (6.8 mL), and the mixture was stirred at room temperature for 6 hours. The reaction solution was concentrated in vacuo and 2N hydrochloric acid was added to the residue to adjust the pH to about 3, thereby crystals were precipitated. The crystals were collected by filtration, washed with cold water and dried in vacuo to give the title compound (411 mg).

Aufarbeitung

  1. concentrationThe reaction solution was concentrated in vacuo and 2N hydrochloric acid
  2. additionwas added to the residue
  3. customcrystals were precipitated
  4. filtrationThe crystals were collected by filtration
  5. washwashed with cold water
  6. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-30674e0652fd4d258c243f1008aa8812
Quelldatensatz
uspto-grants-2009_12
Patentnummer
US07625948B2

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