2-Bromopyridine → HCID 67957992, 화합물
반응식
Br[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.[Li]CCCC.CCCCCC.[CH3:19][C:20]([S:23]([N:25]=[C:26]1[CH2:29][O:28][CH2:27]1)=[O:24])([CH3:22])[CH3:21].C[Al](C)C>C1COCC1.C1(C)C=CC=CC=1>[CH3:22][C:20]([S:23]([NH:25][C:26]1([C:2]2[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=2)[CH2:29][O:28][CH2:27]1)=[O:24])([CH3:19])[CH3:21]참가 물질
반응 조건
- 온도
- -100 °C
실험 절차
To a solution of 2-bromopyridine (0.16 g, 1.02 mmol, 1.0 eq) in dry THF at −100° C. was slowly added a solution of n-BuLi in hexane (2.5M, 0.41 ml, 1.03 mmol, 1 eq), and reaction mixture was then kept in same temperature for 30 minute. A mixture of 2-methyl-N-(oxetan-3-ylidene)propane-2-sulfinamide (0.18 g, 1.02 mmol, 1 eq) and a 2M solution of Me3Al (0.5 ml, 1 mmol, 1 eq) in toluene was stirred at −78° C. for 10 minutes, and then added to the above reaction mixture slowly. The reaction temperature was maintained at −100° C. for another 1 h, after which the reaction mixture warmed to 0° C. slowly. The reaction mixture was quenched with a saturated solution of Na2SO4 and extracted with ethyl acetate. The organic layer was separated and washed with a saturated brine solution, dried over Na2SO4, filtered and the filtrate concentrated. The crude product was purified through a neutral alumina column using 0.5% MeOH/DCM. Yield: 0.1 g (38.5%).
후처리
- additionadded to the above reaction mixture slowly
- temperatureafter which the reaction mixture warmed to 0° C. slowly
- customThe reaction mixture was quenched with a saturated solution of Na2SO4
- extractionextracted with ethyl acetate
- customThe organic layer was separated
- washwashed with a saturated brine solution
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationthe filtrate concentrated
- customThe crude product was purified through a neutral alumina column
출처 및 근거
- ORD 기록
- ord-82b3b1b3345c4a168dd8364fe106455b
- 출처 데이터셋
- uspto-grants-2013_08
- 특허 번호
- US08507683B2
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