Hydrochloric Acid → 1-[3-(4-{4-[1-(2-Chloro-phenyl)-ethoxycarbonylamino]-3-methyl-isoxazol-5-yl}-phenyl)-prop-2-ynyl]-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid

HRID 1253772

Reaktionsgleichung

Reaktionsgleichung von HRID 1253772
C([O:3][C:4]([C:6]1[CH:7]=[N:8][N:9]([CH2:15][C:16]#[C:17][C:18]2[CH:23]=[CH:22][C:21]([C:24]3[O:28][N:27]=[C:26]([CH3:29])[C:25]=3[NH:30][C:31]([O:33][CH:34]([C:36]3[CH:41]=[CH:40][CH:39]=[CH:38][C:37]=3[Cl:42])[CH3:35])=[O:32])=[CH:20][CH:19]=2)[C:10]=1[C:11]([F:14])([F:13])[F:12])=[O:5])C.CO.[OH-].[Li+].Cl>O>[Cl:42][C:37]1[CH:38]=[CH:39][CH:40]=[CH:41][C:36]=1[CH:34]([O:33][C:31]([NH:30][C:25]1[C:26]([CH3:29])=[N:27][O:28][C:24]=1[C:21]1[CH:20]=[CH:19][C:18]([C:17]#[C:16][CH2:15][N:9]2[C:10]([C:11]([F:14])([F:13])[F:12])=[C:6]([C:4]([OH:5])=[O:3])[CH:7]=[N:8]2)=[CH:23][CH:22]=1)=[O:32])[CH3:35]

Komponenten

6

Versuchsvorschrift

To a solution of 1-[3-(4-{4-[1-(2-chloro-phenyl)-ethoxycarbonylamino]-3-methyl-isoxazol-5-yl}-phenyl)-prop-2-ynyl]-5-trifluoromethyl-1H-pyrazole-4-carboxylic acid ethyl ester (0.155 g, 0.26 mmol) in 2:1 MeOH:H2O (3 mL) was added lithium hydroxide (0.033 g, 0.79 mmol), and the reaction was stirred overnight at room temperature. The mixture was acidified with 1N aqueous HCl and extracted with EtOAc, and the combined organic layers were dried, filtered, and concentrated. The residue was purified by preparative HPLC to give the title compound. Mass spec. data (M+H)=573.

Aufarbeitung

  1. extractionextracted with EtOAc
  2. customthe combined organic layers were dried
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified by preparative HPLC

Quellen und Nachweise

ORD-Eintrag
ord-d2eb65d0c7e34f5b98fb68ed7de6226b
Quelldatensatz
uspto-grants-2013_06
Patentnummer
US08455499B2

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