HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 1,3-Diethyl-8-[4-(morpholine-4-sulfonyl)-phenyl]-3,7-dihydro-purine-2,6-dione
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid | HCID 15587300 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1,3-Diethyl-8-[4-(morpholine-4-sulfonyl)-phenyl]-3,7-dihydro-purine-2,6-dione | HCID 15587308 | 54.2% |
Reaction Steps
A mixture of 4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)benzenesulfonic acid (5.0 g, 0.014 moles) and N,N-dimethylformamide (150 ml) is cooled to 0° and treated with thionyl chloride (3.3 g, 0.027 moles). When the addition is complete, the reaction mixture is permitted to warm to ambient temperature and stirred vigorously until a thick slurry results. To this slurry is added morpholine (20 g, 0.23 moles) in one portion. The resulting slurry is stirred one hour and poured into two liters of water. The resulting suspension is filtered, triturated with ethanol, and dried at 68° to yield 3.29 grams of 4-[[4-(1,3-diethyl-2,3,6,7-tetrahydro-2,6-dioxo-1H-purin-8-yl)phenyl]sulfonyl]morpholine, mp 354°-355° C.(d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04452788 |
| Source dataset | uspto-grants-1984_06 |
| ORD ID | ord-5e5d18ea53c3457f870e52e93de46733 |
| Source note | uspto-grants-1984_06 |