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Hydrochloric Acid → 2,4-Dihydroxy-1-(5-[4-(2-[2,2,2-trifluoroethyl]guanidino)pyrimid-2-yl]pentyl)imidazole maleate

HRID 1462345
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1462345
[O-:1][C:2]#N.[K+].[F:5][C:6]([F:28])([F:27])[CH2:7][N:8]=[C:9]([NH2:26])[NH:10][C:11]1[CH:16]=[CH:15][N:14]=[C:13]([CH2:17][CH2:18][CH2:19][CH2:20][CH2:21][NH:22][CH2:23][C:24]#[N:25])[N:12]=1.Cl.[C:30](=[O:33])([O-])[O-:31].[Na+].[Na+].[OH2:36]>CC(O)=O>[C:2]([OH:1])(=[O:36])/[CH:23]=[CH:24]\[C:30]([OH:31])=[O:33].[OH:1][C:2]1[N:22]([CH2:21][CH2:20][CH2:19][CH2:18][CH2:17][C:13]2[N:12]=[C:11]([NH:10][C:9]([NH2:26])=[N:8][CH2:7][C:6]([F:5])([F:27])[F:28])[CH:16]=[CH:15][N:14]=2)[CH:23]=[C:24]([OH:31])[N:25]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 313Hydrochloric AcidHCID 962WaterHCID 10340Sodium CarbonateHCID 11378442Potassium cyanateHCID 202469524-[2-(2,2,2-Trifluoroethyl)guanidino]-2-[5-cyanomethylaminopentyl]pyrimidine

Produkt 1

HCID 178512203
2,4-Dihydroxy-1-(5-[4-(2-[2,2,2-trifluoroethyl]guanidino)pyrimid-2-yl]pentyl)imidazole maleate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 176Acetic AcidLösungsmittel

Versuchsvorschrift

Potassium cyanate (0.055 g.) was added in portions to a solution of 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-[5-cyanomethylaminopentyl]pyrimidine (0.02 g.) in 80% v/v aqueous HOAc (2 ml.) at 0° and the mixture stirred for 1 hour, then heated at 60°-70° for 20 minutes. Concentrated aqueous hydrochloric acid (1 ml.) and water (0.6 ml.) were added and the mixture was heated on a steam bath for 30 minutes. On cooling, saturated sodium carbonate solution was added until the pH was approximately 7. The mixture was extracted with EtOAc, the extract dried (MgSO4) and evaporated. The residue was dissolved in EtOH (4 ml.) and a solution of maleic acid (0.065 g.) in EtOH (0.5 ml.) added. On standing there was obtained 2,4-dihydroxy-1-(5-[4-(2-[2,2,2-trifluoroethyl]guanidino)pyrimid-2-yl]pentyl)imidazole maleate (0.2 g.), m.p. 183°-185°.

Aufarbeitung

  1. temperatureheated at 60°-70° for 20 minutes
  2. temperaturethe mixture was heated on a steam bath for 30 minutes
  3. temperatureOn cooling
  4. extractionThe mixture was extracted with EtOAc
  5. dry with materialthe extract dried (MgSO4)
  6. customevaporated
  7. dissolutionThe residue was dissolved in EtOH (4 ml.)
  8. additiona solution of maleic acid (0.065 g.) in EtOH (0.5 ml.) added

Quellen und Nachweise

ORD-Eintrag
ord-1875b7c52c784565adc6e476daf44b80
Quelldatensatz
uspto-grants-1984_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04460584

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