反応式
ClC1N=CN=C2N(C3C=CC=CC=3)N=CC=12.CCN(CC)CC.N[C@H:25]([CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:26][OH:27]>C(O)C>[C:29]1([CH2:28][CH2:25][CH2:26][OH:27])[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1参加物
5
実験手順
First, 1.13 g of the starting material 4-chloro-1-phenylpyrazolo[3,4-d]pyrimidine was combined with 0.67 ml Et3N, 0.74 g of (R)-(+)-2-amino-3-phenyl-1-propanol in 60 ml absolute ethanol and heated in a steam bath for four hours. The solvent was then removed under vacuum and the residue was purified by flash chromatography (10-20% isopropyl alcohol/hexane) to yield 1.24 g of (R)-β-[1-phenyl-1H-pyrazolo-[3,4-d]pyrimidin-4-yl)amino]benzenepropanol (74% yield).
後処理
- temperatureheated in a steam bath for four hours
- customThe solvent was then removed under vacuum
- customthe residue was purified by flash chromatography (10-20% isopropyl alcohol/hexane)
出典と根拠
- ORDレコード
- ord-911669d008d041b38b40a5cc2bc10729
- 出典データセット
- uspto-grants-1992_02
- 特許番号
- US05086176
関連ノート
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