Toluene → 2-Bromoimidazo[5,1-b]thiazole-7-carbaldehyde
반응식
CON(C)[C:4]([C:6]1[N:7]=[CH:8][N:9]2[CH:13]=[C:12]([Br:14])[S:11][C:10]=12)=[O:5].[H-].C([Al+]CCCC)CCC.C1(C)C=CC=CC=1.C(C(C(C([O-])=O)O)O)([O-])=O.[Na+].[K+]>ClCCl>[Br:14][C:12]1[S:11][C:10]2=[C:6]([CH:4]=[O:5])[N:7]=[CH:8][N:9]2[CH:13]=1참가 물질
실험 절차
A solution of N-methoxy-N-methyl-2-bromoimidazo[5,1-b]thiazole-7-carboxamide (54 mg, 0.19 mmol) in dichloromethane (5 ml) was cooled to −78° C. A solution of dibutylaluminium hydride in toluene (1.01 M solution; 0.4 ml, 0.42 mmol) was added dropwise to the cooled solution, and the mixture was stirred at the same temperature for 3 hr. After the completion of the reaction, a saturated aqueous potassium sodium tartrate solution was added thereto, the mixture was stirred at room temperature for one hr, and the mixture was extracted with ethyl acetate (5 ml×3). The organic layer was washed with saturated brine and was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1) to give 2-bromoimidazo[5,1-b]thiazole-7-carbaldehyde (17 mg, 39%) as a white solid.
후처리
- customAfter the completion of the reaction
- stirringthe mixture was stirred at room temperature for one hr
- extractionthe mixture was extracted with ethyl acetate (5 ml×3)
- washThe organic layer was washed with saturated brine
- dry with materialwas then dried over anhydrous sodium sulfate
- customThe solvent was removed by distillation under the reduced pressure
- customthe residue was purified by column chromatography on silica gel (ethyl acetate:methanol=60:1)
출처 및 근거
- ORD 기록
- ord-44c11f43c44941e5bc3011a775441fd9
- 출처 데이터셋
- uspto-grants-2010_02
- 특허 번호
- US07662841B2
반응 노트
불러오는 중…