4-Benzylpiperazine-1-carboxamidine hemisulfate → HCID 178471120, Verbindung

HRID 1032695Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1032695
[CH:1]([CH:3]([CH:9]([CH3:13])[C:10]([O-:12])=O)[C:4]([O:6][CH2:7][CH3:8])=[O:5])=O.S(O)(O)(=O)=O.[C:19]([N:22]1[CH2:27][CH2:26][N:25]([CH2:28][C:29]2[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=2)[CH2:24][CH2:23]1)(=[NH:21])[NH2:20].C(O[K])(C)(C)C>>[CH2:28]([N:25]1[CH2:24][CH2:23][N:22]([C:19]2[N:21]=[C:10]([OH:12])[C:9]([CH:3]([C:4]([O:6][CH2:7][CH3:8])=[O:5])[CH3:1])=[CH:13][N:20]=2)[CH2:27][CH2:26]1)[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1

Komponenten

4

Versuchsvorschrift

A solution of 2.16 g (10 mmoles) of ethyl 2-formyl-3-methylsuccinate [Zhur. Obshche i Khim., 30, 2250 (1960)] was added to a mixture of 2.67 g (10 mmoles) of 1-amidino-4-benzylpiperazine sulfate, 1.12 g (10 mmoles) of tert-C4H9OK and 12 ml of tert-C4O9OH. The mixture was then refluxed for 6 hours. The reaction mixture was cooled, and extracted by adding water and CHCl3. The CHCl3 layer was dried over anhydrous MgSO4, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (CH2Cl2 :CH3OH=95:5) to give 0.68 g (yield 23%) of 2-(4-benzylpiperazino)-5-(1-ethoxycarbonylethyl)-4-hydroxypyrimidine.

Aufarbeitung

  1. temperatureThe mixture was then refluxed for 6 hours
  2. temperatureThe reaction mixture was cooled
  3. extractionextracted
  4. additionby adding water and CHCl3
  5. dry with materialThe CHCl3 layer was dried over anhydrous MgSO4
  6. customthe solvent was evaporated under reduced pressure
  7. customThe residue was purified by silica gel column chromatography (CH2Cl2 :CH3OH=95:5)

Quellen und Nachweise

ORD-Eintrag
ord-4b85eb89b24b45459510d1a69a365f00
Quelldatensatz
uspto-grants-1990_09
Patentnummer
US04959368

Notizen zur Reaktion

Wird geladen…