Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Homoallyl bromide | HCID 21241 | — |
| Reactant | 3,7-Dihydro-1,3-dimethyl-1H-purine-2,6-dione, sodium salt | HCID 66973603 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13298148 | HCID 13298148 | — |
Reaction Steps
13.9 g of 4-bromo-but-1-ene are reacted with 20.2 g of sodium theophylline in 200 ml of dimethyl-formamide at 120° C. with stirring for approximately 6 to 8 hours until the reaction is complete as indicated by thin-layer chromatography. The solvent is then removed under reduced pressure. The residue is dissolved at 20° C. in 100 ml of methylene chloride, separated from insoluble sodium bromide and purified through a column packed with neutral aluminum oxide to remove small quantities of dark-coloured accompanying substances. Melting point: 110° C. (acetone); yield: 21.6 g (91% of theory relative to the starting material used). After thin-layer chromatography on Merck DC finished plates of silica gel 60 F254 with benzene/acetone (6:4) as eluent, the product has an Rf value of 0.54; and with nitromethane/benzene/pyridine (20:10:3) as eluent, an Rf value of 0.65. Utra-violet light was used as indicator, the pyridine of the eluent having, however, to be removed at 50° C. under reduced pressure because of its property to extinguish fluorescence.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04207321 |
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| Source dataset | uspto-grants-1980_06 |
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| ORD ID | ord-5a5b1dcd0f4a429480a540dbf9f63359 |
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| Source note | uspto-grants-1980_06 |
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