Ethyl oxoacetate → 2,4-Bis[[(2,3-difluorophenyl)methyl]thio]-7(8h)-pteridinone
반응식
[Na].[NH2:2][C:3]1[C:4]([SH:11])=[N:5][C:6]([SH:10])=[N:7][C:8]=1[NH2:9].[F:12][C:13]1[C:20]([F:21])=[CH:19][CH:18]=[CH:17][C:14]=1[CH2:15]Br.C([O:26][CH2:27][CH3:28])(=O)C=O>CO>[F:12][C:13]1[C:20]([F:21])=[CH:19][CH:18]=[CH:17][C:14]=1[CH2:15][S:10][C:6]1[N:5]=[C:4]([S:11][CH2:15][C:14]2[CH:17]=[CH:18][CH:19]=[C:20]([F:21])[C:13]=2[F:12])[C:3]2[N:2]=[CH:28][C:27](=[O:26])[NH:9][C:8]=2[N:7]=1참가 물질
실험 절차
Sodium (3.96 g) was dissolved in methanol (150 ml), 5,6-diamino-2,4-pyrimidinedithiol (15 g) was added, then 2,3-difluorobenzylbromide (30.9 g) slowly added and the reaction mixture was stirred at room temperature under nitrogen for 10 min. Ethyl glyoxalate (15 ml) was added followed by more sodium (2.5 g) and the reaction was left for a further 20 min. The reaction was then quenched with acetic acid (10 ml) and poured on to water (600 ml) with stirring. The resulting precipitate was filtered through celite and washed with water. The filtrate was discarded and the solid was washed through the celite using acetone. The solution was then evaporated to dryness and purified by silica gel column chromatography using 10% ethyl acetate in DCM to yield the sub-titled compound as a cream solid (8 g).
후처리
- waitthe reaction was left for a further 20 min
- customThe reaction was then quenched with acetic acid (10 ml)
- additionpoured on to water (600 ml)
- stirringwith stirring
- filtrationThe resulting precipitate was filtered through celite
- washwashed with water
- washthe solid was washed through the celite
- customThe solution was then evaporated to dryness
- custompurified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-b3ee0dc251c54186a466e4b8017db7ff
- 출처 데이터셋
- uspto-grants-2009_08
- 특허 번호
- US07579342B2
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