Hydrochloric Acid → 3-(5-(3-Chloro-2-(((2',4'-dichloro-[1,1'-biphenyl]-4-yl)amino)methyl)-5-(trifluoromethyl)phenyl)picolinamido)propanoic acid

HRID 405191Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 405191
[OH-].[Na+].C1COCC1.[Cl:8][C:9]1[C:10]([CH2:35][NH:36][C:37]2[CH:42]=[CH:41][C:40]([C:43]3[CH:48]=[CH:47][C:46]([Cl:49])=[CH:45][C:44]=3[Cl:50])=[CH:39][CH:38]=2)=[C:11]([C:19]2[CH:20]=[CH:21][C:22]([C:25]([NH:27][CH2:28][CH2:29][C:30]([O:32]CC)=[O:31])=[O:26])=[N:23][CH:24]=2)[CH:12]=[C:13]([C:15]([F:18])([F:17])[F:16])[CH:14]=1.Cl>CCOC(C)=O.[Na+].[Cl-].CO>[Cl:8][C:9]1[C:10]([CH2:35][NH:36][C:37]2[CH:42]=[CH:41][C:40]([C:43]3[CH:48]=[CH:47][C:46]([Cl:49])=[CH:45][C:44]=3[Cl:50])=[CH:39][CH:38]=2)=[C:11]([C:19]2[CH:20]=[CH:21][C:22]([C:25]([NH:27][CH2:28][CH2:29][C:30]([OH:32])=[O:31])=[O:26])=[N:23][CH:24]=2)[CH:12]=[C:13]([C:15]([F:16])([F:17])[F:18])[CH:14]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
40 °C

Versuchsvorschrift

A 3M aqueous solution of NaOH (3.1 mL, 9.3 mmol) was added to a THF (12.6 mL) and MeOH (6.3 mL) solution of ethyl 3-(5-(3-chloro-2-(((2′,4′-dichloro-[1,1′-biphenyl]-4-yl)amino)methyl)-5-(trifluoromethyl)phenyl)picolinamido)propanoate (4.1 g, 6.3 mmol) and the resulting homogeneous mixture was heated to 40° C. After 30 min the resulting mixture was acidified with 6M aqueous HCl (1.6 mL, 9.6 mmol) diluted with EtOAc and 4M aqueous NaCl, and the layers were separated. The aqueous layer was extracted with EtOAc and the combined organics were washed with 4M NaCl, dried (Na2SO4), concentrated, and purified via HPLC to yield the title compound.

Aufarbeitung

  1. customthe layers were separated
  2. extractionThe aqueous layer was extracted with EtOAc
  3. washthe combined organics were washed with 4M NaCl
  4. dry with materialdried (Na2SO4)
  5. concentrationconcentrated
  6. custompurified via HPLC

Quellen und Nachweise

ORD-Eintrag
ord-e77e4fcada0449a7bf3ec23e5dbabbd1
Quelldatensatz
uspto-grants-2014_06
Patentnummer
US08748624B2

Notizen zur Reaktion

Wird geladen…