Hydrochloric Acid → 2-Amino-9-(2-hydroxyethoxymethyl)adenine hydrochloride
Reaction equation
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:11][O:12][CH2:13][CH2:14][OH:15])=[C:4]([NH2:16])[N:3]=1.[ClH:17].CCOCC>C(O)C>[ClH:17].[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:11][O:12][CH2:13][CH2:14][OH:15])=[C:4]([NH2:16])[N:3]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-Amino-9-(2-hydroxyethoxymethyl)adenine (0.25g) was dissolved in hot ethanol (50ml) and the solution cooled in an ice bath. To the cool solution was added sufficient HCl-saturated ethanol to give a pH of 1.0. Dry ether (50ml) was then added and the mixture thoroughly chilled. The resulting flesh-colored solid was removed by filtration and washed with cold ethanol. Recrystallization from methanol yielded 2-amino-9-(2-hydroxyethoxymethyl)adenine hydrochloride (0.21g., 74% of theoretical), m.p. 207°-211° C. Elemental analysis and NMR support this structure.
Workup
- temperaturethe solution cooled in an ice bath
- customto give a pH of 1.0
- temperaturethe mixture thoroughly chilled
- customThe resulting flesh-colored solid was removed by filtration
- washwashed with cold ethanol
- customRecrystallization from methanol
Sources & evidence
- ORD record
- ord-5db7cafeee5a4d8da09e7f118b6c2d6b
- Source dataset
- uspto-grants-1979_03
- Patent number
- US04146715
Reaction notes
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