2-Bromoethanol → HCID 22346783、化合物
反応式
[I:1][C:2]1[C:10]2[C:5](=[N:6][CH:7]=[N:8][C:9]=2[NH2:11])[NH:4][N:3]=1.[H-].[Na+].Br[CH2:15][CH2:16][OH:17]>CN(C=O)C>[NH2:11][C:9]1[N:8]=[CH:7][N:6]=[C:5]2[N:4]([CH2:15][CH2:16][OH:17])[N:3]=[C:2]([I:1])[C:10]=12参加物
反応条件
- 温度
- 50 °C
実験手順
To a solution of 3-iodo-1H-pyrazolo[3,4-d]pyrimidin-4-amine (5.00 g, 19.1 mmol) in DMF (40 mL) was added sodium hydride (60%, 1.53 g, 38.3 mmol) and the reaction mixture was stirred for 20 min. 2-bromoethanol (1.50 mL, 21.1 mmol) was added and the reaction mixture was heated at 50° C. for 18 h. The reaction mixture was cooled to ambient temperature and concentrated to afford a brown sludge. Ice water (50 mL) was added and the resulting precipitate was collected by filtration, rinsed with water (50 mL) and ether (50 mL), and dried in vacuo to afford 2-(4-amino-3-iodo-1H-pyrazolo[3,4-d]pyrimidin-1-yl)-1-ethanol as a beige solid (4.30 g, 14.1 mmol): 1H NMR (d6-DMSO, 400 MHz): δH 8.19 (1H, s), 4.84 (1H, t, J=5.8 Hz), 4.30 (1H, t, J=5.8 Hz), and 3.77 (2H, app q, J=5.6 Hz); RP-HPLC (Hypersil C18, 5 μm, 100 Å, 15 cm; 5%-100% acetonitrile-0.1 M ammonium acetate over 15 min, 1 mL/min). Rt 7.35 min.
後処理
- temperatureThe reaction mixture was cooled to ambient temperature
- concentrationconcentrated
- customto afford a brown sludge
- filtrationthe resulting precipitate was collected by filtration
- washrinsed with water (50 mL) and ether (50 mL)
- customdried in vacuo
出典と根拠
- ORDレコード
- ord-c22fdcee6262481eb629800df5e08ef6
- 出典データセット
- uspto-grants-2005_07
- 特許番号
- US06921763B2
反応ノート
読み込み中…