반응식
C([N-]C(C)C)(C)C.[Li+].[CH3:9][N:10]1[C:15](=[O:16])[C:14]2[CH:17]=[CH:18][S:19][C:13]=2[N:12]([CH2:20][CH:21]([CH3:23])[CH3:22])[C:11]1=[O:24].[CH3:25][N:26]1[C:30]2[CH:31]=[CH:32][CH:33]=[CH:34][C:29]=2[N:28]=[C:27]1[CH:35]=[O:36]>O1CCCC1>[OH:36][CH:35]([C:18]1[S:19][C:13]2[N:12]([CH2:20][CH:21]([CH3:22])[CH3:23])[C:11](=[O:24])[N:10]([CH3:9])[C:15](=[O:16])[C:14]=2[CH:17]=1)[C:27]1[N:26]([CH3:25])[C:30]2[CH:31]=[CH:32][CH:33]=[CH:34][C:29]=2[N:28]=1참가 물질
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A solution of lithium diisopropylamide (3.15 mmol) in anhydrous tetrahydrofuran (5 ml) was added to a solution of 3-methyl-1-(2-methylpropyl)thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (500 mg) in anhydrous tetrahydrofuran (20 ml) at −78° C. After 10 minutes, 1-methylbenzimidazole-2-carboxaldehyde (600 mg) was added and the resultant solution kept at −78° C. for 1 hour. The reaction mixture was allowed to warm to ambient temperature and quenched with saturated sodium hydrogen carbonate solution. The mixture was extracted with ethyl acetate and washed with saturated sodium hydrogen carbonate and then brine, then dried over a mixture of magnesium sulfate and silica, filtered, and evaporated. Purification by HPLC over silica eluting with an isohexane:ethyl acetate gradient (4:1 to 0:1) gave the title compound (0.13 g).
후처리
- customquenched with saturated sodium hydrogen carbonate solution
- extractionThe mixture was extracted with ethyl acetate
- washwashed with saturated sodium hydrogen carbonate
- dry with materialbrine, then dried over a mixture of magnesium sulfate and silica
- filtrationfiltered
- customevaporated
- customPurification by HPLC over silica eluting with an isohexane
출처 및 근거
- ORD 기록
- ord-a42dadee039c4c8cab9e92fadd8430e2
- 출처 데이터셋
- uspto-grants-2001_10
- 특허 번호
- US06300334B1
연결된 노트
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