반응식
[CH3:1][CH:2]([CH3:25])[CH2:3][CH2:4][O:5][C:6]1[N:14]=[C:13]2[C:9]([N:10]=[C:11]([O:22]C)[N:12]2[CH2:15][CH:16]2[CH2:21][CH2:20][O:19][CH2:18][CH2:17]2)=[C:8]([NH2:24])[N:7]=1.Cl.[OH-].[Na+]>CO.O1CCOCC1>[NH2:24][C:8]1[N:7]=[C:6]([O:5][CH2:4][CH2:3][CH:2]([CH3:25])[CH3:1])[N:14]=[C:13]2[C:9]=1[NH:10][C:11](=[O:22])[N:12]2[CH2:15][CH:16]1[CH2:17][CH2:18][O:19][CH2:20][CH2:21]1참가 물질
6
실험 절차
To a solution of 2-[(3-methylbutyl)oxy]-8-methoxy-9-(tetrahydro-2H-pyran-4-ylmethyl)-9H-purin-6-amine (52 mg) in dry MeOH (5.7 mL) was added 4N HCl in 1,4-dioxane (0.971 mL) and the reaction mixture was stirred at room temperature for 3 h. The reaction was neutralised to pH7 with 2M sodium hydroxide solution and concentrated in vacuo to give a white solid. The solid was washed with water (20 mL) and was filtered under reduced pressure to give the title compound as an off-white solid (31 mg).
후처리
- concentrationconcentrated in vacuo
- customto give a white solid
- washThe solid was washed with water (20 mL)
- filtrationwas filtered under reduced pressure
출처 및 근거
- ORD 기록
- ord-65ef9de3cb044d3a9fea865cf66cb271
- 출처 데이터셋
- uspto-grants-2011_07
- 특허 번호
- US07977344B2
연결된 노트
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