Hydrochloric Acid → 5-[(2-oxo-2,3-dihydro-1H-indol-4-ylmethyl)-carbamoyl]-3-trifluoromethyl-thiophene-2-carboxylic acid

HRID 1952602Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1952602
C[O:2][C:3]([C:5]1[S:6][C:7]([C:14](=[O:27])[NH:15][CH2:16][C:17]2[CH:25]=[CH:24][CH:23]=[C:22]3[C:18]=2[CH2:19][C:20](=[O:26])[NH:21]3)=[CH:8][C:9]=1[C:10]([F:13])([F:12])[F:11])=[O:4].O.[OH-].[Li+].C1COCC1.Cl>O>[O:26]=[C:20]1[CH2:19][C:18]2[C:22](=[CH:23][CH:24]=[CH:25][C:17]=2[CH2:16][NH:15][C:14]([C:7]2[S:6][C:5]([C:3]([OH:4])=[O:2])=[C:9]([C:10]([F:13])([F:11])[F:12])[CH:8]=2)=[O:27])[NH:21]1

Komponenten

6

Versuchsvorschrift

A mixture of 5-[(2-oxo-2,3-dihydro-1H-indol-4-ylmethyl)-carbamoyl]-3-trifluoromethyl-thiophene-2-carboxylic acid methyl ester (270 mg, 0.68 mmol), lithium hydroxide monohydrate (280 mg, 6.77 mmol), THF (5 mL) and water (5 mL) was stirred 15 h, acidified with 1N HCl and extracted with EtOAc (×3). The organic extracts were combined, washed with brine, dried over sodium sulfate, filtered and evaporated to give the title compound, 260 mg (99%). MS m/e 354.9 (M+H+).

Aufarbeitung

  1. extractionextracted with EtOAc (×3)
  2. washwashed with brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-6bfba90f9048442080b35567accb0eb8
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08404859B2

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