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Ammonia → 1,1-Diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]urea

HRID 231709
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 231709
C(O[CH2:4][CH3:5])=O.[CH:6]([SH:9])([SH:8])[CH3:7].[CH2:10]([N:12]([CH2:33][CH3:34])[C:13]([NH:15][C@H:16]1[CH2:30][C@H:29]2[C@@H:19]([CH2:20][C:21]3[C:31]4[C:24](=[CH:25][CH:26]=[CH:27][C:28]2=4)[NH:23]C=3)[N:18]([CH3:32])[CH2:17]1)=[O:14])[CH3:11].N>C(Cl)(Cl)Cl.[Ti](Cl)(Cl)(Cl)Cl.O.CO>[CH2:33]([N:12]([CH2:10][CH3:11])[C:13]([NH:15][C@H:16]1[CH2:30][C@H:29]2[C@@H:19]([CH2:20][C:21]3[C:31]4[C:24](=[CH:25][CH:26]=[CH:27][C:28]2=4)[NH:23][C:7]=3[CH:6]2[S:9][CH2:5][CH2:4][S:8]2)[N:18]([CH3:32])[CH2:17]1)=[O:14])[CH3:34]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 222AmmoniaHCID 8025Ethyl formateHCID 336451,1-EthanedithiolHCID 443951Terguride

Produkt 1

HCID 867420541,1-Diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]ureaAusbeute 42 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 24193
Titanium Tetrachloride
Katalysator
HCID 887MethanolLösungsmittel
HCID 962WaterLösungsmittel
HCID 6212ChloroformLösungsmittel2×

Versuchsvorschrift

At room temperature under argon, 7 ml of ethyl formate and 3.6 ml (44 mmol) of ethanedithiol are added in succession to a solution of 6.8 g of 1,1-diethyl-3-(6-methyl-8α-ergolinyl)urea in 200 ml of chloroform. Thereafter 8.8 ml (80 mmol) of titanium(IV) chloride dissolved in 100 ml of chloroform is added gradually dropwise to the mixture. The latter is stirred for 20 hours at room temperature. Although the starting material is not as yet entirely converted at this point in time, the reaction mixture is worked up to avoid further formation of the disubstituted compound. For this purpose, the reaction mixture is cooled in an ice bath and combined, in sequence, dropwise with 50 ml of methanol and 40 ml of water. The mixture is then made alkaline with 25% ammonia solution and extracted with methylene chloride. The organic phases are washed with water and dried over magnesium sulfate. The evaporated residue is crystallized in boiling heat from methanol/ethyl acetate, thus obtaining 3.8 g of 1,1-diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8α-ergolinyl]urea (42% yield).

Aufarbeitung

  1. additionis added gradually dropwise to the mixture
  2. temperatureFor this purpose, the reaction mixture is cooled in an ice bath
  3. extractionextracted with methylene chloride
  4. washThe organic phases are washed with water
  5. dry with materialdried over magnesium sulfate
  6. customThe evaporated residue is crystallized
  7. temperaturein boiling heat from methanol/ethyl acetate

Quellen und Nachweise

ORD-Eintrag
ord-f5f5ba45034d40d79cd3c367248f3e5e
Quelldatensatz
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04847262

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