Bromine → diethyl 4-((6-amino-8-bromo-2-(2-methoxyethoxy)-9H-purin-9-yl)methyl)benzylphosphonate

HRID 629931노트

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HRID 629931 반응식
[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][O:14][CH3:15])[N:8]=[C:7]2[C:3]=1[N:4]=[CH:5][N:6]2[CH2:16][C:17]1[CH:31]=[CH:30][C:20]([CH2:21][P:22](=[O:29])([O:26][CH2:27][CH3:28])[O:23][CH2:24][CH3:25])=[CH:19][CH:18]=1.C([O-])(=O)C.[Na+].[Br:37]Br>C(O)(=O)C>[NH2:1][C:2]1[N:10]=[C:9]([O:11][CH2:12][CH2:13][O:14][CH3:15])[N:8]=[C:7]2[C:3]=1[N:4]=[C:5]([Br:37])[N:6]2[CH2:16][C:17]1[CH:31]=[CH:30][C:20]([CH2:21][P:22](=[O:29])([O:23][CH2:24][CH3:25])[O:26][CH2:27][CH3:28])=[CH:19][CH:18]=1

참가 물질

5

실험 절차

To a solution of diethyl 4-((6-amino-2-(2-methoxyethoxy)-9H-purin-9-yl)methyl)benzylphosphonate (1 equiv.) in acetic acid (0.20 M) was added sodium acetate (15 equiv.) and bromine (13 equiv.). The reaction mixture was then allowed to stir at room temperature for 18 h. At this point the reaction was quenched by the addition of sodium thiosulfate. The mixture was then diluted with water and DCM. This mixture was transferred to a separatory funnel and washed with DCM three times. The combined organic layers were then dried over anhydrous Na2SO4 and the volatiles were removed in vacuo. The resulting residue was purified by a COMBIFLASH™ system using a gradient of 0-5% MeOH/DCM to provide the title compound (14%) as a solid.

후처리

  1. customAt this point the reaction was quenched by the addition of sodium thiosulfate
  2. additionThe mixture was then diluted with water and DCM
  3. customThis mixture was transferred to a separatory funnel
  4. washwashed with DCM three times
  5. dry with materialThe combined organic layers were then dried over anhydrous Na2SO4
  6. customthe volatiles were removed in vacuo
  7. customThe resulting residue was purified by a COMBIFLASH™ system

출처 및 근거

ORD 기록
ord-6ffe0737b7204f399e1a37eb3ecbed8d
출처 데이터셋
uspto-grants-2016_04
특허 번호
US09315530B2

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