Hydrogen Peroxide → HCID 20475751、化合物
反応式
[OH:1]O.[O:3]1[CH2:14][CH:4]1[CH2:5][S:6][C:7]1[N:12]=[CH:11][C:10]([Cl:13])=[CH:9][N:8]=1.[Na+].[Cl-]>O.CO>[O:3]1[CH2:14][CH:4]1[CH2:5][S:6]([C:7]1[N:8]=[CH:9][C:10]([Cl:13])=[CH:11][N:12]=1)=[O:1]参加物
6
実験手順
A mixture of 35% H2O2 (1.9 mmol) and SeO2 (1.9 mmol) in water (1.5 ml H2O) was added to a solution of 2-(2,3-epoxypropyl)thio-5-chloropyrimidine (1.9 mmol) in methanol (7 ml). The mixture was stirred at room temperature for 4 h before saturated NaCl aq. (30 ml) was added and the mixture extracted with chloroform (3×15 ml). The dried (MgSO4) chloroform solution was evaporated and the residue purified by preparative TLC on silica gel using CHCl3 : EtOH (95:5); yield 24%, m.p. 92° C. 1H NMR (CDCl3): δ2.4-3.6 (5H, m), 8.84 (H-4, H-6). IR (KBr): 1050 cm-1 (SO).
後処理
- additionwas added
- extractionthe mixture extracted with chloroform (3×15 ml)
- dry with materialThe dried (MgSO4) chloroform solution
- customwas evaporated
- customthe residue purified by preparative TLC on silica gel
出典と根拠
- ORDレコード
- ord-7d83328fb76640d7b22cfa5ef561b5ef
- 出典データセット
- uspto-grants-1983_12
- 特許番号
- US04423047
反応ノート
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