Ammonia → N2 (3-methoxyphenylacetyl)-2'-deoxyguanosine

HRID 54639

Reaktionsgleichung

Reaktionsgleichung von HRID 54639
[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.[CH3:25][O:26][C:27]1[CH:28]=[C:29]([CH2:33][C:34](Cl)=[O:35])[CH:30]=[CH:31][CH:32]=1.[NH3:37]>N1C=CC=CC=1.O>[N:37]#[N:9].[CH3:25][O:26][C:27]1[CH:28]=[C:29]([CH2:33][C:34]([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:35])[CH:30]=[CH:31][CH:32]=1

Komponenten

7

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To dry 2'-deoxyguanosine (1) (14.2 g, 50 mmoles) in 300 ml of dry pyridine at 0° C. was added trimethylsilyl chloride (33 ml, 250 mmoles) and the mixture stirred at 0° C. for 1 hour. 3-Methoxyphenylacetyl chloride (40 ml, 250 mmoles) was added and the solution maintained at room temperature for 15 hours. The reaction mixture was then cooled in an ice bath and 50 ml of cold water was added. After 30 minutes, 50 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 400 ml water and 400 ml methylene chloride in a separating funnel. The product crystallized out of the aqueous solution upon extraction with CH2Cl2 was filtered off, washed with CH2Cl2 (3×50 ml) and ether (3×50 ml) and air dried to yield 15.56 g (75%) of N2 -(3-methoxyphenylacetyl)-2'-deoxyguanosine (2b), as confirmed by spectroscopic and elemental analysis.

Aufarbeitung

  1. temperaturethe solution maintained at room temperature 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 400 ml water
  7. customThe product crystallized out of the aqueous solution upon extraction with CH2Cl2
  8. filtrationwas filtered off
  9. washwashed with CH2Cl2 (3×50 ml) and ether (3×50 ml) and air
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-2beef6d9805c485f9593c5e6dac7e3f9
Quelldatensatz
uspto-grants-1997_04
Patentnummer
US05623068

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