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Hydrogen Bromide → Bromocriptine

HRID 2309788
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 2309788
[BrH:1].[OH-].[Na+].[CH3:4][CH:5]([CH2:7][C@@H:8]1[N:17]2[C:18]([C@@:20]([NH:25][C:26]([C@@H:28]3[CH:43]=[C:42]4[C@@H:31]([CH2:32][C:33]5[C:37]6[C:38]4=[CH:39][CH:40]=[CH:41][C:36]=6[NH:35][CH:34]=5)[N:30]([CH3:44])[CH2:29]3)=[O:27])([CH:22]([CH3:24])[CH3:23])[O:21][C@@:16]2([OH:45])[C@H:15]2[N:11]([CH2:12][CH2:13][CH2:14]2)[C:9]1=[O:10])=[O:19])[CH3:6].[OH-].[NH4+]>CS(C)=O.ClCCl.O>[CH3:6][CH:5]([CH2:7][C@@H:8]1[N:17]2[C:18]([C@@:20]([NH:25][C:26]([C@@H:28]3[CH:43]=[C:42]4[C@@H:31]([CH2:32][C:33]5[C:37]6[C:36](=[CH:41][CH:40]=[CH:39][C:38]=64)[NH:35][C:34]=5[Br:1])[N:30]([CH3:44])[CH2:29]3)=[O:27])([CH:22]([CH3:23])[CH3:24])[O:21][C@@:16]2([OH:45])[C@H:15]2[N:11]([CH2:12][CH2:13][CH2:14]2)[C:9]1=[O:10])=[O:19])[CH3:4]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 260Hydrogen Bromide6×HCID 14798Sodium HydroxideHCID 14923Ammonium HydroxideHCID 134551Ergocryptine2×

Produkt 1

HCID 31101Bromocriptine

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 679
Dimethyl Sulfoxide
Lösungsmittel
4×
HCID 962WaterLösungsmittel
HCID 6344DichloromethaneLösungsmittel

Versuchsvorschrift

Dry gaseous hydrogen bromide is introduced to 70 ml. of anhydrous dimethylsulphoxide at room temperature. The amount of the introduced hydrogen bromide is measured by titrating against 0.1N sodium hydroxide solution. The hydrogen bromide is introduced until reaching a hydrogen bromide content of 0.0003 to 0.0005 mole/ml. in the dimethylsulphoxide. Then 10 g (0.01737 mole) of α-ergocryptine are dissolved in an amount containing 12 equivalents of hydrogen bromide as taken out from the thus-obtained mixture containing hydrogen bromide in dimethylsulphoxide. The reaction mixture is stirred at room temperature for 15 minutes beginning from the complete dissolution of α-ergocryptine, then poured in 5 volumes of water as calculated for the volume of dimethylsulphoxide. Then the mixture is alkalinized to a pH value of 8 to 9 by adding ammonium hydroxide, the precipitated 2-bromo-α-ergocryptine is filtered off, washed twice with 10 ml. of water each, dissolved in 200 ml. of dichloromethane and dried over anhydrous sodium sulphate. After filtering off the drying agent, 200 ml. of diisopropyl ether are added to the solution and dichloromethane is distilled off under atmospheric pressure. 2-bromo-αergocryptine separated from the distillation residue is filtered off and washed to give a yield of 8.4 g. (74%), m. p.: 215°-217° C., [α]D20 =-190° c=1%, dichloromethane).

Aufarbeitung

  1. customat room temperature
  2. filtrationthe precipitated 2-bromo-α-ergocryptine is filtered off
  3. washwashed twice with 10 ml
  4. dissolutionof water each, dissolved in 200 ml
  5. dry with materialof dichloromethane and dried over anhydrous sodium sulphate
  6. filtrationAfter filtering off the drying agent, 200 ml
  7. additionof diisopropyl ether are added to the solution and dichloromethane
  8. distillationis distilled off under atmospheric pressure
  9. custom2-bromo-αergocryptine separated from the distillation residue
  10. filtrationis filtered off
  11. washwashed
  12. customto give a yield of 8.4 g

Quellen und Nachweise

ORD-Eintrag
ord-e4a16ff9a8094d23a2ede0a690351b05
Quelldatensatz
uspto-grants-1987_09
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04697017

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