Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | 4-Nitrobenzaldehyde | HCID 541 | — |
| Reactant | 5,6-Diamino-1,3-dipropyl-2,4(1H,3H)-pyrimidinedione | HCID 5098605 | — |
| Reactant | 8-(4-Nitrophenyl)-1,3-dipropyl-3,7-dihydro-1H-purine-2,6-dione | HCID 14257871 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 21285789 | HCID 21285789 | — |
Reaction Steps
1,3-Dipropyl-8-(4-nitrophenyl)xanthine, was prepared by treatment of 1,3-dipropyl-5,6-diaminouracil (1.01 g, 4.5 mmol) with 4-nitrobenzaldehyde (0.85 g, 5.6 mmol) in absolute ethanol (50 ml) in the presence of acetic acid (0.6 ml) and heated at reflux for 1 hour to yield 1,3-dipropyl-5-amino-6-(4-nitrophenyl)iminouracil. Treatment of 1,3-dipropyl-5-amino-6-(4-nitrophenyl)iminouracil (1.2 g, 3.3 mmol) with diethyl azodicarboxylate (7 ml) at 90° C. in toluene (40 ml) gave after dilution with ethanol a precipitate. This precipitate was recrystallized from ethanol yielding 0.95 g of pure product (81%). IR (KBr) 3180 (N--H), 1710(C=O), 1650(C=O), 1520(C=C) cm-1 ; Anal. Calcd. for C17H19N5O4 : MW 357.38: C, 57.14; H, 5.36; N, 19.60. Found: C, 57.22; H, 5.42; N, 19.50.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04783530 |
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| Source dataset | uspto-grants-1988_11 |
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| ORD ID | ord-7a56a2a213d24ae1b5fa0330b8cedd67 |
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| Source note | uspto-grants-1988_11 |
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