Hydrochloric Acid → 3-(5-(2-(((2-Chloro-2'-methyl-4'-(trifluoromethyl)-[1,1'-biphenyl]-4-yl)amino)methyl)-3-isopropyl-5-(trifluoromethyl)phenyl)picolinamido)propanoic acid
Reaktionsgleichung
[OH-].[Na+].C1COCC1.[Cl:8][C:9]1[CH:14]=[C:13]([NH:15][CH2:16][C:17]2[C:22]([CH:23]([CH3:25])[CH3:24])=[CH:21][C:20]([C:26]([F:29])([F:28])[F:27])=[CH:19][C:18]=2[C:30]2[CH:31]=[CH:32][C:33]([C:36]([NH:38][CH2:39][CH2:40][C:41]([O:43]CC)=[O:42])=[O:37])=[N:34][CH:35]=2)[CH:12]=[CH:11][C:10]=1[C:46]1[CH:51]=[CH:50][C:49]([C:52]([F:55])([F:54])[F:53])=[CH:48][C:47]=1[CH3:56].Cl>CO>[Cl:8][C:9]1[CH:14]=[C:13]([NH:15][CH2:16][C:17]2[C:22]([CH:23]([CH3:24])[CH3:25])=[CH:21][C:20]([C:26]([F:28])([F:29])[F:27])=[CH:19][C:18]=2[C:30]2[CH:31]=[CH:32][C:33]([C:36]([NH:38][CH2:39][CH2:40][C:41]([OH:43])=[O:42])=[O:37])=[N:34][CH:35]=2)[CH:12]=[CH:11][C:10]=1[C:46]1[CH:51]=[CH:50][C:49]([C:52]([F:55])([F:53])[F:54])=[CH:48][C:47]=1[CH3:56]Komponenten
6
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A 3M aqueous NaOH solution (0.04 mL, 0.11 mmol) was added to a THF (2.0 mL) and MeOH (1.0 mL) solution of ethyl 3-(5-(2-(((2-chloro-2′-methyl-4′-(trifluoromethyl)-[1,1′-biphenyl]-4-yl)amino)methyl)-3-isopropyl-5-(trifluoromethyl)phenyl)picolinamido)propanoate (13 mg, 0.02 mmol) and the resulting mixture was stirred at room temperature. After 2 h the resulting mixture was acidified with 1N aqueous HCl and extracted with EtOAc. The combined organics were dried (Na2SO4), concentrated and purified via column chromatography to yield the title compound.
Aufarbeitung
- extractionextracted with EtOAc
- dry with materialThe combined organics were dried (Na2SO4)
- concentrationconcentrated
- custompurified via column chromatography
Quellen und Nachweise
- ORD-Eintrag
- ord-dc3567e0a98f438c96add42999726cc2
- Quelldatensatz
- uspto-grants-2014_06
- Patentnummer
- US08748624B2
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