반응식
[NH2:1][C:2]1[N:7]=[C:6]([C:8]([OH:10])=O)[CH:5]=[C:4]([C:11]2[O:12][CH:13]=[CH:14][CH:15]=2)[N:3]=1.[NH:16]1[C:24]2[C:19](=[CH:20][C:21]([CH2:25][NH2:26])=[CH:22][CH:23]=2)[CH:18]=[CH:17]1.N=C=N.O.ON1C2C=CC=CC=2N=N1>CN(C=O)C>[NH2:1][C:2]1[N:7]=[C:6]([C:8]([NH:26][CH2:25][C:21]2[CH:20]=[C:19]3[C:24](=[CH:23][CH:22]=2)[NH:16][CH:17]=[CH:18]3)=[O:10])[CH:5]=[C:4]([C:11]2[O:12][CH:13]=[CH:14][CH:15]=2)[N:3]=1참가 물질
6
실험 절차
A mixture consisting of 2-amino-6-(2-furyl)pyrimidine-4-carboxylic acid (206 mg, 1.0 mmol), indole-5-methanamine (146 mg, 1.0 mmol), polymer supported carbodiimide (Argonaut Technologies, loading 1.38 mmol/g, 1.10 g, 1.5 mmol) and 1-hydroxybenzotriazole hydrate (203 mg, 1.5 mmol) in DMF (5 mL) was stirred at room temperature for 24 hr. The mixture was filtered through a pad of Celite, washing through with EtOAc. The filtrate was washed successively with H2O (10 mL), 2-M Na2CO3 (2×10 mL) and H2O (10 mL), dried (MgSO4) and concentrated in vacuo. The resulting oil was dissolved in MeOH (1.0 mL), added dropwise with stirring to H2O (2 mL) and the resulting precipitate filtered to give the title compound (198 mg, 59%) as a cream solid.
후처리
- filtrationThe mixture was filtered through a pad of Celite
- washwashing through with EtOAc
- washThe filtrate was washed successively with H2O (10 mL), 2-M Na2CO3 (2×10 mL) and H2O (10 mL)
- dry with materialdried (MgSO4)
- concentrationconcentrated in vacuo
- dissolutionThe resulting oil was dissolved in MeOH (1.0 mL)
- additionadded dropwise
- stirringwith stirring to H2O (2 mL)
- filtrationthe resulting precipitate filtered
출처 및 근거
- ORD 기록
- ord-9cc58eadd0584f6a90a024859fd625e1
- 출처 데이터셋
- uspto-grants-2011_01
- 특허 번호
- US07875600B2
연결된 노트
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