HuagongsheHuagongshe Chemistry Print Report · For research reference only
Toluene → N4-undecyloxycarbonyl-1-beta-D-arabinofuranosylcytosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Toluene | HCID 1140 | — |
| Reactant | 2(1H)-Pyrimidinone, 4-amino-1-arabinofuranosyl- | HCID 114682 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Undecyloxycarbonyl chloride | HCID 20513604 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | N4-undecyloxycarbonyl-1-beta-D-arabinofuranosylcytosine | HCID 13090287 | 30.4% |
Reaction Steps
In 130 ml of dimethylacetamide, 7.3 g of arabinofuranosylcytosine is dissolved and to the resultant solution is added 40 ml of a toluene solution containing 7.56 g of sodium hydrogen carbonate and 7.0 g of undecyloxycarbonyl chloride. The mixture is then stirred at room temperature for 3 hours. After the reaction is over, the solvent is removed under reduced pressure and ice-water is added to the residue, whereby the cyrstals are precipitated. The crystals are filtered and washed with water, followed by sufficient drying. Recrystallization of the product is performed twice, using 80 ml of chloroform-n-hexane, to give 4.0 g of N4-undecyloxycarbonyl-1-β-D-arabinofuranosylcytosine (Yield:30%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04367332 |
| Source dataset | uspto-grants-1983_01 |
| ORD ID | ord-1a4b8043bfa3411c81e2b8358b178cef |
| Source note | uspto-grants-1983_01 |