Methyl methoxyacetate → 1-[5-Chloro-4-(tetrahydro-pyran-2-yloxymethyl)-pyridin-3-yl]-2-methoxy-ethanone
반응식
Br[C:2]1[CH:3]=[N:4][CH:5]=[C:6]([Cl:16])[C:7]=1[CH2:8][O:9][CH:10]1[CH2:15][CH2:14][CH2:13][CH2:12][O:11]1.[Li]CCCC.[CH3:22][O:23][C:24](=O)[CH2:25][O:26]C.C([O-])(O)=O.[Na+]>C1COCC1>[Cl:16][C:6]1[C:7]([CH2:8][O:9][CH:10]2[CH2:15][CH2:14][CH2:13][CH2:12][O:11]2)=[C:2]([C:25](=[O:26])[CH2:24][O:23][CH3:22])[CH:3]=[N:4][CH:5]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
3-Bromo-5-chloro-4-(tetrahydro-pyran-2-yloxymethyl)-pyridine (0.30 g, 0.98 mmol) was dissolved in anhydrous THF (15 mL) under Ar and the solution was cooled to −78° C. n-BuLi (0.62 mL, 1.6 M in hexanes, 0.98 mmol) was added dropwise and the reaction mixture was stirred at −78° C. for 0.5 h. Then methoxy-acetic acid methyl ester (0.97 mL, 9.8 mmol) dissolved in anhydrous THF (10 mL) was added dropwise and stirring was continued at −78° C. for 2 h. At completion of the reaction, monitored by TLC, saturated NaHCO3 was added with vigorous stirring. The quenched mixture was extracted with EA (2×20 mL) and the combined organic extracts were washed with saturated NaHCO3 (20 mL) and dried over Na2SO4. The residue was purified by flash chromatography on silica gel with EA/hexane to provide the title compound as a colorless oil. MS (m/z): 300.5 [M+H+].
후처리
- additionwas added dropwise
- additionwas added dropwise
- stirringstirring
- waitwas continued at −78° C. for 2 h
- customAt completion of the reaction
- additionwas added with vigorous stirring
- extractionThe quenched mixture was extracted with EA (2×20 mL)
- washthe combined organic extracts were washed with saturated NaHCO3 (20 mL)
- dry with materialdried over Na2SO4
- customThe residue was purified by flash chromatography on silica gel with EA/hexane
출처 및 근거
- ORD 기록
- ord-00e94146245944e0907b4e3c7a36cfe1
- 출처 데이터셋
- uspto-grants-2013_04
- 특허 번호
- US08410134B2
반응 노트
불러오는 중…