Reaction equation
[NH:1]1[C:10](=[O:11])[C:9]2[NH:8][CH:7]=[N:6][C:5]=2[N:4]=[C:2]1[NH2:3].[CH:12]([CH:14]=[O:15])=[O:13]>O>[CH:12]([CH:14]=[O:15])=[O:13].[NH:1]1[C:10](=[O:11])[C:9]2[NH:8][CH:7]=[N:6][C:5]=2[N:4]=[C:2]1[NH2:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 70 °C
Procedure
22.65 g of guanine (manufactured by Tokyo Kasei Kogyo Co.) and 21.75 g of a 40% glyoxal aqueous solution (manufactured by Tokyo Kasei Kogyo Co.) were added to 950 mL of purified water, and the mixture was stirred with heating at 70° C. for 18 hours. The mixture was then cooled to 4° C. and filtered. The white solid obtained by the filtration was dried, thereby resulting in 30.7 g of glyoxal-guanine. The measurement result of nuclear magnetic resonance (NMR) spectrum is as follows:
Workup
- temperatureThe mixture was then cooled to 4° C.
- filtrationfiltered
- customThe white solid obtained by the filtration
- customwas dried
- customresulting in 30.7 g of glyoxal-guanine
- customThe measurement result of nuclear magnetic resonance (NMR) spectrum
Sources & evidence
- ORD record
- ord-ae4be01da311443db89272a348963be3
- Source dataset
- uspto-grants-2006_11
- Patent number
- US07141397B2
Linked notes
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