Diltiazem → cis-3-(Acetyloxy)-2,3,4,5-tetrahydro-2-(4-methoxyphenyl)-N-[2-(3,5-dimethoxyphenyl)ethyl]-N,N-dimethyl-4-oxo-1,5-benzothiazepine-5-ethanaminium iodide

HRID 568784Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 568784
[CH3:1][C:2]([O:4][C@H:5]1[C:15](=[O:16])[N:14]([CH2:17][CH2:18][N:19]([CH3:21])[CH3:20])[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[S:7][C@H:6]1[C:22]1[CH:23]=[CH:24][C:25]([O:28][CH3:29])=[CH:26][CH:27]=1)=[O:3].[CH3:30][O:31][C:32]1[CH:33]=[C:34]([CH:38]=[C:39]([O:41][CH3:42])[CH:40]=1)[CH2:35][CH2:36][I:37]>CCOC(C)=O>[I-:37].[C:2]([O:4][C@H:5]1[C:15](=[O:16])[N:14]([CH2:17][CH2:18][N+:19]([CH2:36][CH2:35][C:34]2[CH:38]=[C:39]([O:41][CH3:42])[CH:40]=[C:32]([O:31][CH3:30])[CH:33]=2)([CH3:21])[CH3:20])[C:13]2[CH:12]=[CH:11][CH:10]=[CH:9][C:8]=2[S:7][C@H:6]1[C:22]1[CH:23]=[CH:24][C:25]([O:28][CH3:29])=[CH:26][CH:27]=1)(=[O:3])[CH3:1]

Komponenten

4

Reaktionsbedingungen

Temperatur
50 °C

Versuchsvorschrift

To a flask under nitrogen was added 5.0 g (0.0121 mole) of diltiazem, 3.52 g (0.0121 mole) of 3,5-dimethoxyphenethyl iodide, and 20 ml of EtOAc. The reaction mixture was heated at 50° C. for 24 hr then at 75° C. for 97 hr. The reaction was cooled to RT, the solvent decanted, and the oily residue washed three times with EtOAc. The oily residue was dissolved in methylene chloride, washed with water and dried over MgSO4. The solvent was evaporated to give 5.45 g of a mixture of the title product and diltiazem hydroiodide as a tan foam.

Aufarbeitung

  1. temperatureThe reaction was cooled to RT
  2. customthe solvent decanted
  3. washthe oily residue washed three times with EtOAc
  4. dissolutionThe oily residue was dissolved in methylene chloride
  5. washwashed with water
  6. dry with materialdried over MgSO4
  7. customThe solvent was evaporated

Quellen und Nachweise

ORD-Eintrag
ord-5867a41daf9544d99acdef383e874dc3
Quelldatensatz
uspto-grants-1988_03
Patentnummer
US04729994

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