반응식
[NH:1]1[CH2:6][CH2:5][O:4][C@H:3]([CH2:7][NH:8][C:9]2[C:18]3[C:13](=[N:14][CH:15]=[CH:16][N:17]=3)[CH:12]=[C:11]([C:19]3[CH:24]=[CH:23][C:22]([N:25]4[CH2:30][CH2:29][O:28][CH2:27][CH2:26]4)=[CH:21][CH:20]=3)[N:10]=2)[CH2:2]1.Br[C:32]1[N:37]=[CH:36][CH:35]=[CH:34][N:33]=1.C(=O)([O-])[O-].[Cs+].[Cs+]>CN(C=O)C>[O:28]1[CH2:29][CH2:30][N:25]([C:22]2[CH:21]=[CH:20][C:19]([C:11]3[N:10]=[C:9]([NH:8][CH2:7][C@H:3]4[O:4][CH2:5][CH2:6][N:1]([C:32]5[N:37]=[CH:36][CH:35]=[CH:34][N:33]=5)[CH2:2]4)[C:18]4[C:13](=[N:14][CH:15]=[CH:16][N:17]=4)[CH:12]=3)=[CH:24][CH:23]=2)[CH2:26][CH2:27]1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
A solution of (S)—N-(morpholin-2-ylmethyl)-7-(4-morpholinophenyl)pyrido[4,3-b]pyrazin-5-amine (100 mg, 0.246 mmol), 2-bromopyrimidine (59 mg, 0.37 mmol) and cesiumcarbonate (193 mg, 0.592 mmol) in DMF (2 mL) was heated at 100° C. in a sealed tube for overnight. Then the mixture was extracted with EA, washed with brine, concentrated and purified by flash column chromatography, eluting with DCM/MeOH to give product as light yellow solid. MS (m/z): 485 (M+H)+
후처리
- extractionThen the mixture was extracted with EA
- washwashed with brine
- concentrationconcentrated
- custompurified by flash column chromatography
- washeluting with DCM/MeOH
- customto give product as light yellow solid
출처 및 근거
- ORD 기록
- ord-ef64dc99c85f443da08f1a0eda8e388a
- 출처 데이터셋
- uspto-grants-2016_09
- 특허 번호
- US09434726B2
연결된 노트
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