Dimethyl Sulfoxide → 4-(7-Chloroquinolin-4-yl)butyraldehyde
반응식
C(Cl)(=O)C(Cl)=O.CS(C)=O.[Cl:11][C:12]1[CH:21]=[C:20]2[C:15]([C:16]([CH2:22][CH2:23][CH2:24][CH2:25][OH:26])=[CH:17][CH:18]=[N:19]2)=[CH:14][CH:13]=1.C(N(CC)CC)C>C(Cl)Cl>[Cl:11][C:12]1[CH:21]=[C:20]2[C:15]([C:16]([CH2:22][CH2:23][CH2:24][CH:25]=[O:26])=[CH:17][CH:18]=[N:19]2)=[CH:14][CH:13]=1참가 물질
반응 조건
- 온도
- -78 °C
실험 절차
Oxalyl chloride (0.42 mL of a 2M solution in dry methylene chloride) was placed in an oven-dried flask, cooled to -78° C. and a solution of 99 mg methylsulfoxide in dry methylene chloride (2 mL) added drop by drop to the oxalyl chloride over 3 minutes and stirred for a further 3 minutes. A solution of 4-(7-chloroquinolin-4-yl)butan-1-ol (100 mg) in dry methylene chloride (1 mL) was added to the reaction flask over approx. 3 minutes followed by anhydrous triethylamine (0.42 mL) and the reaction mixture stirred for another 2.5 hours during which time it was allowed warmed up to room temperature. The reaction was quenched by the addition of saturated brine and then partitioned with methylene chloride. The aqueous layer was discarded and the methylene chloride extract dried over anhydrous sodium sulfate powder, filtered and concentrated in vacuo. The title compound was isolated by flash chromatography on silica gel (ethyl acetate:hexane, 2:1; then ethyl acetate), 57 mg.
후처리
- stirringthe reaction mixture stirred for another 2.5 hours during which time it
- temperaturewas allowed warmed up to room temperature
- customThe reaction was quenched by the addition of saturated brine
- custompartitioned with methylene chloride
- extractionthe methylene chloride extract
- dry with materialdried over anhydrous sodium sulfate powder
- filtrationfiltered
- concentrationconcentrated in vacuo
출처 및 근거
- ORD 기록
- ord-cb0d1846999c48b7b3ba7a03c6b96910
- 출처 데이터셋
- uspto-grants-2000_12
- 특허 번호
- US06156767
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