2-Bromoethanol → HCID 22346783, 화합물
반응식
[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]=12참가 물질
반응 조건
- 온도
- 50 °C
실험 절차
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.
후처리
- 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
출처 및 근거
- ORD 기록
- ord-c22fdcee6262481eb629800df5e08ef6
- 출처 데이터셋
- uspto-grants-2005_07
- 특허 번호
- US06921763B2
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