Methyl Methanesulfonate → 1-(2-Hydroxyethyl)-2-methylthio-3,4,5,6-tetrahydropyrimidine mesylate
反応式
[OH:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH2:7][NH:6][C:5]1=[S:10].[CH3:11][S:12]([O:15]C)(=[O:14])=[O:13]>C(O)C.COC(C)(C)C>[S:12]([OH:15])(=[O:14])(=[O:13])[CH3:11].[OH:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][CH2:7][NH:6][CH:5]1[S:10][CH3:11]参加物
5
実験手順
Then, 1-(2-hydroxyethyl)-3,4,5,6-tetrahydropyrimidine-2-thione (121.2 g) and methyl methanesulfonate (91.51 g) are heated at reflux in ethyl alcohol (200 ml) for about 2 hours and then allowed to cool to room temperature. The mixture was diluted with t-butyl methyl ether (2 liters). An oil separates which crystallizes on keeping in freezer at -20° C. Filtration and drying yields 145.7 g of 1-(2-hydroxyethyl)-2-methylthio-3,4,5,6-tetrahydropyrimidine mesylate, melting point 61.7°-62.2° C.
後処理
- customAn oil separates which crystallizes
- customon keeping in freezer at -20° C
- filtrationFiltration
- customdrying
出典と根拠
- ORDレコード
- ord-333625bfe3524323baec2a941c41e1f7
- 出典データセット
- uspto-grants-1993_11
- 特許番号
- US05258381
反応ノート
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