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Ammonia → N2 (phenylacetyl)-2'-deoxyguanosine

HRID 54637
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 54637
[C@@H:1]1([N:9]2[C:19]3[N:18]=[C:16]([NH2:17])[NH:15][C:13](=[O:14])[C:12]=3[N:11]=[CH:10]2)[O:8][C@H:5]([CH2:6][OH:7])[C@@H:3]([OH:4])[CH2:2]1.C[Si](Cl)(C)C.[C:25]1([CH2:31][C:32](Cl)=[O:33])[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.[NH3:35]>N1C=CC=CC=1.O>[N:35]#[N:9].[C:25]1([CH2:31][C:32]([C@@:1]2([N:9]3[C:19]4[N:18]=[C:16]([NH2:17])[NH:15][C:13](=[O:14])[C:12]=4[N:11]=[CH:10]3)[O:8][C@H:5]([CH2:6][OH:7])[C@@H:3]([OH:4])[CH2:2]2)=[O:33])[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 4

HCID 222AmmoniaHCID 6397ChlorotrimethylsilaneHCID 7679Phenylacetyl chlorideHCID 135398592Deoxyguanosine

Produkt 1

HCID 136381139N2 (phenylacetyl)-2'-deoxyguanosineAusbeute 56 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962
Water
Lösungsmittel
HCID 1049PyridineLösungsmittel2×

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

2'-Deoxyguanosine (1)(32.5 g, 120 mmoles) was dried three times by co-evaporation with dried pyridine and suspended in 700 ml of dry pyridine. To this suspension at 0° C. trimethylsilyl chloride (80 ml, 600 mmoles) was added and the mixture stirred at 0° C. for 1 hour. Phenylacetyl chloride (80 ml, 600 mmoles) was added dropwise and the solution stirred for 15 hours. The reaction mixture was then cooled in an ice bath and 150 ml of cold water was added. After 30 minutes, 150 ml of 29% aqueous ammonia was added and the mixture stirred for 30 minutes. The solution was then evaporated to near dryness and the residue dissolved in 700 ml water and 700 ml methylene chloride. The product crystallized out of the aqueous solution upon extraction with CH2Cl2 was filtered off, washed with CH2Cl2 (3×70 ml) and ether (3×70 ml) and air dried to yield 27 g (56%) of N2 -(phenylacetyl)-2'-deoxyguanosine (2a), as confirmed by spectroscopic and elemental analysis.

Aufarbeitung

  1. stirringthe solution stirred for 15 hours
  2. temperatureThe reaction mixture was then cooled in an ice bath
  3. waitAfter 30 minutes
  4. stirringthe mixture stirred for 30 minutes
  5. customThe solution was then evaporated
  6. dissolutionthe residue dissolved in 700 ml water
  7. customThe product crystallized out of the aqueous solution upon extraction with CH2Cl2
  8. filtrationwas filtered off
  9. washwashed with CH2Cl2 (3×70 ml) and ether (3×70 ml) and air
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-bfad6452c2c247f38b63f1246f8e4234
Quelldatensatz
uspto-grants-1997_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05623068

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