HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-(methoxymethoxymethyl)-1,8-dihydropteridine-4,7-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 178499629 | HCID 178499629 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-(methoxymethoxymethyl)-1,8-dihydropteridine-4,7-dione | HCID 178499622 | — |
Reaction Steps
1.1 g (0.00464 mole) of 4-amino-7-hydroxy-2-(methoxymethoxymethyl)pteridine is added to a solution of 1.5 g (0.0267 mole) of potassium hydroxide in 20 ml of water. The mixture is refluxed for 8 hours. After cooling, the reaction mixture is acidified with 10% hydrochloric acid to pH 5.5. The precipitate formed is isolated by filtration and washed with water. It is extracted with a mixture of 50 ml of ethanol and 60 ml of N,N-dimethylformamide under reflux. This extract, concentrated under reduced pressure, is recrystallized from a mixture of ethanol and N,N-dimethylformamide. Yld: 0.2 g (18%), m.p. 224°-226° C. (ethanol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05270465 |
| Source dataset | uspto-grants-1993_12 |
| ORD ID | ord-f8fe38af6ed84826bd8d460826ec6e86 |
| Source note | uspto-grants-1993_12 |