Trifluoroacetic acid → 1-[3-(2-Isopropyloxyethylamino)benzoyl]-4-[2-(4-chlorophenyl)ethyl]piperazine hydrochloride

HRID 1975372Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1975372
FC(F)(F)C(O)=O.[CH:8]([O:11][CH2:12][CH2:13][N:14]([C:22]1[CH:23]=[C:24]([CH:42]=[CH:43][CH:44]=1)[C:25]([N:27]1[CH2:32][CH2:31][N:30]([CH2:33][CH2:34][C:35]2[CH:40]=[CH:39][C:38]([Cl:41])=[CH:37][CH:36]=2)[CH2:29][CH2:28]1)=[O:26])C(OC(C)(C)C)=O)([CH3:10])[CH3:9]>ClCCl>[ClH:41].[CH:8]([O:11][CH2:12][CH2:13][NH:14][C:22]1[CH:23]=[C:24]([CH:42]=[CH:43][CH:44]=1)[C:25]([N:27]1[CH2:32][CH2:31][N:30]([CH2:33][CH2:34][C:35]2[CH:36]=[CH:37][C:38]([Cl:41])=[CH:39][CH:40]=2)[CH2:29][CH2:28]1)=[O:26])([CH3:10])[CH3:9]

Komponenten

4

Versuchsvorschrift

65 ml of trifluoroacetic acid are introduced into 100 ml of dichloromethane. A solution of 7.2 g of 1-{3-[N-(2-isopropyloxyethyl)-N-tert-butoxycarbonylamino]benzoyl}-4-[2-(4-chlorophenyl)ethyl]piperazine is added thereto within a period of 5 minutes. After 2 hours at RT, the reaction solution is concentrated by evaporation and the residue is neutralised with sodium hydroxide solution and extracted with ether. Concentration by evaporation and treatment with ethereal hydrochloric acid yield 1-[3-(2-isopropyloxyethylamino)benzoyl]-4-[2-(4-chlorophenyl)ethyl]piperazine hydrochloride having a melting point of 157°-159°.

Aufarbeitung

  1. waitAfter 2 hours at RT
  2. concentrationthe reaction solution is concentrated by evaporation
  3. extractionextracted with ether
  4. concentrationConcentration
  5. customby evaporation and treatment with ethereal hydrochloric acid

Quellen und Nachweise

ORD-Eintrag
ord-8bccc7971f2244fbabec8f4d36b6f81b
Quelldatensatz
uspto-grants-1994_02
Patentnummer
US05286728

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