Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-6-chloropurine | HCID 5360349 | — |
| Reactant | HCID 53809709 | HCID 53809709 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20431321 | HCID 20431321 | — |
Reaction Steps
Equimolar amounts of 2-amino-6-chloropurine, 4-bromoethyl-1,3-dioxane (prepared according to Price C. C. J. Amer. Chem. Soc. 1950, 72, 5335-6) and anhydrous potassium carbonate were mixed in dry dimethyl formamide. After stirring for seven days at room temperature the mixture was filtered and the filtrate evaporated at reduced pressure. The residue was triturated with hot ethanol and undissolved material filtered off. The filtrate was evaporated to dryness and a yellow crystalline solid was obtained which was recrystallized from chloroform to give colourless rod-shaped crystalls. M.p. 169°-70° C. (uncorr.) UV Spectra (hydrochloric acid 0.01 mol/l): λmax (nm) 308, 245. UV spectra (ethanol): λmax (nm) 310, 247. M.S.: 11.2 a J., m/e (int): 271/269 (0.19/0.55), 226/224 (0.11/0.28) 212/210 (0.38/0.82) 171/169 (0.35/1.0)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04495190 |
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| Source dataset | uspto-grants-1985_01 |
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| ORD ID | ord-ace8b4263a93447380b2b1eef8beee86 |
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| Source note | uspto-grants-1985_01 |
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