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tert-Butanol → HCID 136181547, Verbindung

HRID 848717
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 848717
[P:1]([O:5][C@@H:6]1[C@@H:10]([CH2:11][OH:12])[O:9][C@@H:8]([N:13]2[C:23]3[N:22]=[C:20]([NH2:21])[NH:19][C:17](=[O:18])[C:16]=3[N:15]=[CH:14]2)[C@@H:7]1[OH:24])(O)([OH:3])=[O:2].C(O)(C)(C)C.C1([N:36]=C=NC2CCCCC2)CCCCC1>O.N.C(N)=O>[P:1]([O:5][C@@H:6]1[C@@H:10]([CH2:11][OH:12])[O:9][C@@H:8]([N:13]2[C:23]3[N:22]=[C:20]([NH2:21])[NH:19][C:17](=[O:18])[C:16]=3[N:15]=[CH:14]2)[C@@H:7]1[OH:24])([NH2:36])(=[O:2])[OH:3]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 3

HCID 6386tert-ButanolHCID 10868DicyclohexylcarbodiimideHCID 1353987273'-Gmp

Produkt 1

HCID 136181547HCID 136181547, VerbindungAusbeute 50 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 713FormamideLösungsmittel
HCID 12896473
Azane;hydrate
Lösungsmittel

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

Three millimoles of guanosine-3'-monophosphate were dissolved in a mixture of 7.5 ml of 2 N ammonia water and 5 ml of formamide, the solution was combined with 20 ml of tertiary butanol that contained 15 millimoles of dicyclohexyl carbodiimide, and the resulting mixture was heated at 80° C. for a period of 9 to 10 hours with care taken to prevent evaporation of the solvent. After the reaction, the mixture was left to stand overnight at room temperature, the precipitate was filtered off, the filtrate was concentrated under vacuum to remove the tertiary butanol, and the residue was extracted with ether. The aqueous layer was recovered, concentrated under vacuum, and the residue was treated with acetone to give a crystal of guanosine-3'-monophosphoramidate in a yield of about 50%. The crystal was heated under vacuum at 100° C. for a period of 3 to 4 hours until it was dehydrated thoroughly.

Aufarbeitung

  1. customevaporation of the solvent
  2. customAfter the reaction
  3. waitthe mixture was left
  4. filtrationthe precipitate was filtered off
  5. concentrationthe filtrate was concentrated under vacuum
  6. customto remove the tertiary butanol
  7. extractionthe residue was extracted with ether
  8. customThe aqueous layer was recovered
  9. concentrationconcentrated under vacuum
  10. additionthe residue was treated with acetone

Quellen und Nachweise

ORD-Eintrag
ord-5b8ab559fab44be59b1a9b64a6a36ec8
Quelldatensatz
uspto-grants-1981_10
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04297347

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