반응식
[Li]CCCC.CCN(C(C)C)C(C)C.[Cl:15][C:16]1[CH:25]=[CH:24][C:23]2[C:18](=[CH:19][C:20]([C:26]([F:29])([F:28])[F:27])=[CH:21][CH:22]=2)[N:17]=1.[C:30](=[O:32])=[O:31]>C1COCC1>[Cl:15][C:16]1[C:25]([C:30]([OH:32])=[O:31])=[CH:24][C:23]2[C:18](=[CH:19][C:20]([C:26]([F:28])([F:27])[F:29])=[CH:21][CH:22]=2)[N:17]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
11 ml of BuLi (1M in hexane) were added dropwise at −78° C. to a solution of 1.9 ml (11 mmol) of DIPEA in THF (77 ml). After stirring for 30 min at −78° C., a solution of 2.31 g (10 mmol) of 2-chloro-7-(trifluoromethyl)quinoline in THF (30 ml) was added and stirring was carried out for a further 30 min at −78° C. The reaction solution was then poured onto finely divided, solid CO2. After heating to RT, most of the THF was removed in vacuo. A 1M aq. NaOH soln. was then added and the phases were separated. The aqueous phase was acidified with 10% hydrochloric acid and extracted with EA. The organic phase was washed with water and brine, dried over Na2SO4, filtered and concentrated in vacuo. There were obtained as residue 2.12 g (7.7 mmol, 71%) of 2-chloro-7-(trifluoromethyl)quinoline-3-carboxylic acid, which was reacted further without additional purification.
후처리
- stirringstirring
- waitwas carried out for a further 30 min at −78° C
- additionThe reaction solution was then poured
- customwas removed in vacuo
- additionwas then added
- customthe phases were separated
- extractionextracted with EA
- washThe organic phase was washed with water and brine
- dry with materialdried over Na2SO4
- filtrationfiltered
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-d1802e31d2f249cd96009f8b41521c67
- 출처 데이터셋
- uspto-grants-2012_06
- 특허 번호
- US08207342B2
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