Sodium Hydroxide → 1-Butanol, 2-(4-pyrimidinylamino)-
反応式
Cl[C:2]1[N:7]=[CH:6][N:5]=[C:4]([NH:8][CH:9]([CH2:12][CH3:13])[CH2:10][OH:11])[CH:3]=1.[OH-].[Na+]>C(O)C.[Pd]>[N:7]1[CH:2]=[CH:3][C:4]([NH:8][CH:9]([CH2:12][CH3:13])[CH2:10][OH:11])=[N:5][CH:6]=1参加物
5
実験手順
2-[(6-Chloro-4-pyrimidinyl)amino]-1-butanol was dissolved in ethanol (110 mL), which was sequentially added with a 5N aqueous sodium hydroxide solution (5.5 mL) and Pd—C (hydrous product; 0.55 g), and hydrogenation was performed under hydrogen atmosphere at a normal temperature and a normal pressure. After completion of the reaction, Pd—C was filtered off, and the solvent was evaporated. The resulting residue was extracted with dichloromethane-methanol, and the solvent was removed to give the title compound (4.3 g) as white crystals.
後処理
- filtrationwas filtered off
- customthe solvent was evaporated
- extractionThe resulting residue was extracted with dichloromethane-methanol
- customthe solvent was removed
出典と根拠
- ORDレコード
- ord-7aeaa9b5e887432ea2aa67e82af68d84
- 出典データセット
- uspto-grants-2006_07
- 特許番号
- US07078405B2
反応ノート
読み込み中…