반응식
[NH2:1][C:2]1[CH:12]=[CH:11][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:4][CH:3]=1.[N:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][C:21]=2[S:23](Cl)(=[O:25])=[O:24])[CH:16]=[CH:15][CH:14]=1>N1C=CC=CC=1>[N:13]1[C:22]2[C:17](=[CH:18][CH:19]=[CH:20][C:21]=2[S:23]([NH:1][C:2]2[CH:3]=[CH:4][C:5]([C:6]([O:8][CH2:9][CH3:10])=[O:7])=[CH:11][CH:12]=2)(=[O:25])=[O:24])[CH:16]=[CH:15][CH:14]=1참가 물질
4
실험 절차
To a stirred solution of ethyl 4-aminobenzoate (5 gm, 30.3 mmol) under nitrogen atmosphere was added pyridine (50 ml) at 0° C. and stirred for 10 min. Quinoline-8-sulfonyl chloride 89 (8.94 gm, 39.4 mmol) was then added to the reaction mixture at the same temperature. The resulting mixture was stirred for 16 hr at RT. After completion of the reaction, the solvent was removed under low pressure. The traces of pyridine were removed by co-distillation with toluene. Diethylether was added to the resulting residue, and the solid product was filtered out and air-dried. The resulting crude product (8.0 gm, 74%) was taken to the next step without further purification.
후처리
- stirringThe resulting mixture was stirred for 16 hr at RT
- customAfter completion of the reaction
- customthe solvent was removed under low pressure
- customThe traces of pyridine were removed by co-distillation with toluene
- additionDiethylether was added to the resulting residue
- filtrationthe solid product was filtered out and
- customair-dried
- customThe resulting crude product (8.0 gm, 74%) was taken to the next step without further purification
출처 및 근거
- ORD 기록
- ord-29c0526d4c6140309f840f68b3b62a0f
- 출처 데이터셋
- uspto-grants-2014_07
- 특허 번호
- US08785450B2
연결된 노트
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