Hydrochloric Acid → N-[2-(4-Carboxymethoxyphenyl)-1-methylethyl]-N-(2-hydroxyethyl)-2-hydroxy-2-(2-trifluoromethyl-thiazol-4-yl)ethanamine

HRID 1587947Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1587947
[C:1]([CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH:14]([N:16]([CH2:29][CH2:30][OH:31])[CH2:17][CH:18]([OH:28])[C:19]2[N:20]=[C:21]([C:24]([F:27])([F:26])[F:25])[S:22][CH:23]=2)[CH3:15])=[CH:9][CH:8]=1)([O:3]C)=[O:2].[OH-].[Na+].Cl>CO>[C:1]([CH2:5][O:6][C:7]1[CH:12]=[CH:11][C:10]([CH2:13][CH:14]([N:16]([CH2:29][CH2:30][OH:31])[CH2:17][CH:18]([OH:28])[C:19]2[N:20]=[C:21]([C:24]([F:27])([F:25])[F:26])[S:22][CH:23]=2)[CH3:15])=[CH:9][CH:8]=1)([OH:3])=[O:2]

Komponenten

5

Versuchsvorschrift

Prepared by analogy to Example 16 by reaction of N-[2-(4-carbomethoxymethoxyphenyl)-1-methylethyl]-N-(2-hydroxyethyl)-2-hydroxy-2-(2-trifluoromethyl-thiazol-4-yl)ethanamine in methanol with 1N sodium hydroxide solution. After the mixture has been neutralised with 1N hydrochloric acid it is evaporated to dryness, treated with 10 ml of ethanol, and the inorganic residues are removed by filtration. The ethanol phase is diluted with 60 ml of methylene chloride and again filtered. The mother liquor is evaporated to dryness, and the residue is triturated with ether and filtered off with suction.

Aufarbeitung

  1. customis evaporated to dryness
  2. additiontreated with 10 ml of ethanol
  3. customthe inorganic residues are removed by filtration
  4. additionThe ethanol phase is diluted with 60 ml of methylene chloride
  5. filtrationagain filtered
  6. customThe mother liquor is evaporated to dryness
  7. customthe residue is triturated with ether
  8. filtrationfiltered off with suction

Quellen und Nachweise

ORD-Eintrag
ord-2ecd9d5eecc84deb90dfd37619bd9057
Quelldatensatz
uspto-grants-1993_06
Patentnummer
US05219852

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