8-azido-7-(4-chlorobenzyl)-3-methyl-1-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-1H-purine-2,6(3H,7H)-dione → 8-amino-7-(4-chlorobenzyl)-3-methyl-1-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-1H-purine-2,6(3H,7H)-dione
반응식
[N:1]([C:4]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[CH:16][CH:15]=2)[C:11]2[C:10](=[O:21])[N:9]([CH2:22][CH2:23][CH2:24][O:25][CH:26]3[CH2:31][CH2:30][CH2:29][CH2:28][O:27]3)[C:8](=[O:32])[N:7]([CH3:33])[C:6]=2[N:5]=1)=[N+]=[N-].[H][H]>C1COCC1.[Pd]>[NH2:1][C:4]1[N:12]([CH2:13][C:14]2[CH:15]=[CH:16][C:17]([Cl:20])=[CH:18][CH:19]=2)[C:11]2[C:10](=[O:21])[N:9]([CH2:22][CH2:23][CH2:24][O:25][CH:26]3[CH2:31][CH2:30][CH2:29][CH2:28][O:27]3)[C:8](=[O:32])[N:7]([CH3:33])[C:6]=2[N:5]=1참가 물질
5
반응물 2
생성물 1
시약·촉매·용매 2
실험 절차
8-azido-7-(4-chlorobenzyl)-3-methyl-1-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-1H-purine-2,6(3H,7H)-dione (0.19 g, 0.4 mmol) was dissolved in THF (5 mL) and 10% Pd/C (20 mg) was added. The reaction was blanketed in a hydrogen atmosphere (balloon) and stirred overnight at room temperature. The mixture was filtered through celite, the filter cake was washed with methanol. The filtrate was concentrated in vacuo to give a 8-amino-7-(4-chlorobenzyl)-3-methyl-1-(3-(tetrahydro-2H-pyran-2-yloxy)propyl)-1H-purine-2,6(3H,7H)-dione (0.2 g, 100% yield) as a white solid. LCMS retention time 1.324 min; LCMS MH+-THP 364
후처리
- filtrationThe mixture was filtered through celite
- washthe filter cake was washed with methanol
- concentrationThe filtrate was concentrated in vacuo
출처 및 근거
- ORD 기록
- ord-2e518c2ba15d442faa61d59a0f3c74bd
- 출처 데이터셋
- uspto-grants-2016_06
- 특허 번호
- US09359359B2
반응 노트
불러오는 중…