반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1.Br.[OH-].[Na+].[CH3:12][O:13][C:14]([C:16]1[NH:17][C:18]2[C:23]([C:24]=1[CH:25]=[O:26])=[CH:22][CH:21]=[C:20]([O:27][CH3:28])[CH:19]=2)=[O:15].C([O-])([O-])=O.[K+].[K+]>CCOCC.CN(C=O)C>[CH:25]([C:24]1[C:23]2[C:18](=[CH:19][C:20]([O:27][CH3:28])=[CH:21][CH:22]=2)[N:17]([CH2:2][C:3]2[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=2)[C:16]=1[C:14]([O:13][CH3:12])=[O:15])=[O:26]참가 물질
8
반응물 5
생성물 1
시약·촉매·용매 2
반응 조건
- 온도
- 60 °C
실험 절차
General Procedure J. 2-Bromomethylpyridine.HBr salt (7.0 g, 27.7 mmol) was treated with NaOH (4M, 6.9 ml, 27.6 mmol) in Et2O (20 ml). The ether layer was separated, washed with brine, and dried over MgSO4, filtered into a flask containing a suspension of methyl3-formyl-6-methoxy-1H-indole-2-carboxylate (Compound 90, 1.29 g, 5.54 mmol) and K2CO3 (2.3 g, 16.6 mmol) in DMF (25 ml). The reaction was stirred at 60° C. for 3 h, cooled to room temperature, quenched with H2O and extracted with EtOAc (×2). The combined organic layer was washed with brine, dried over Na2SO4, and concentrated in vacuo. The residue was purified by washing with H2O (×3) and filtration to yield the title compound as a golden brown solid.
후처리
- customThe ether layer was separated
- washwashed with brine
- dry with materialdried over MgSO4
- filtrationfiltered into a flask
- additioncontaining
- temperaturecooled to room temperature
- customquenched with H2O
- extractionextracted with EtOAc (×2)
- washThe combined organic layer was washed with brine
- dry with materialdried over Na2SO4
- concentrationconcentrated in vacuo
- customThe residue was purified
- washby washing with H2O (×3) and filtration
출처 및 근거
- ORD 기록
- ord-eb22265ff8ae48ce943d2a17ad525da2
- 출처 데이터셋
- uspto-grants-2013_09
- 특허 번호
- US08524917B2
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