Ethylene Glycol → HCID 67263330, compound
Reaction equation
[Na].Cl[C:3]1[N:11]=[C:10]2[C:6]([N:7]=[CH:8][N:9]2[CH2:12][C:13]2[CH:14]=[N:15][C:16]([CH3:19])=[CH:17][CH:18]=2)=[C:5]([NH2:20])[N:4]=1.O.[CH2:22]([OH:25])[CH2:23][OH:24]>>[OH:24][CH2:23][CH2:22][O:25][C:3]1[N:11]=[C:10]2[C:6]([N:7]=[CH:8][N:9]2[CH2:12][C:13]2[CH:14]=[N:15][C:16]([CH3:19])=[CH:17][CH:18]=2)=[C:5]([NH2:20])[N:4]=1Participants
5
Conditions
- Temperature
- 100 °C
Procedure
After sodium (2.1 g, 91 mmol) was dissolved in ethylene glycol (30 ml), 2-chloro-9-{(6-methyl3-pyridyl)methyl}adenine (3.0 g, 11 mmol) was added thereto and the mixture was stirred at 100° C. for 3 hours. After the mixture was allowed to cool, water (80 ml) was added thereto and the resulting precipitate was filtered to give the captioned compound (3.1 g, 10 mmol, yield: 94%) as a white solid.
Workup
- temperatureto cool
- filtrationthe resulting precipitate was filtered
Sources & evidence
- ORD record
- ord-9f649b5f7b98481f8961e7804d82c7fb
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07754728B2
Reaction notes
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