Ammonium Chloride → HCID 66636981, 화합물
반응식
[Br-].[CH2:2]([O:9][CH2:10][CH2:11][CH2:12][P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[K].CC(C)([O-])C.[CH:38]1([NH:44][C:45]2[CH:54]=[C:53]3[C:48]([C:49](=[O:62])[C:50]([CH:60]=O)=[CH:51][N:52]3[CH:55]([CH2:58][CH3:59])[CH2:56][CH3:57])=[CH:47][C:46]=2[F:63])[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]1.[Cl-].[NH4+]>C1COCC1>[CH2:2]([O:9][CH2:10][CH2:11][CH:12]=[CH:60][C:50]1[C:49](=[O:62])[C:48]2[C:53](=[CH:54][C:45]([NH:44][CH:38]3[CH2:39][CH2:40][CH2:41][CH2:42][CH2:43]3)=[C:46]([F:63])[CH:47]=2)[N:52]([CH:55]([CH2:56][CH3:57])[CH2:58][CH3:59])[CH:51]=1)[C:3]1[CH:4]=[CH:5][CH:6]=[CH:7][CH:8]=1참가 물질
실험 절차
To a 20 ml THF suspension of 1081 mg of (3-benzyloxypropyl)triphenylphosphonium bromide was added 258 mg of potassium, tert-butoxide followed by stirring for 1.5 hours. A 10 ml THF solution of 358 mg of 7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoro-4-oxo-1,4-dihydroquinoline-3-carbaldehyde was added thereto, followed by stirring for 1 hour. To the reaction mixture was added aqueous saturated ammonium chloride, followed by extraction with ethyl acetate and washing with aqueous saturated sodium chloride. After drying over anhydrous sodium sulfate and subsequent concentration under a reduced pressure, the residue was purified by silica gel column chromatography to obtain 488 mg of 3-[4-(benzyloxy)but-1-en-1-yl]-7-(cyclohexylamino)-1-(1-ethylpropyl)-6-fluoroquinolin-4(1H)-one.
후처리
- stirringby stirring for 1 hour
- extractionfollowed by extraction with ethyl acetate
- washwashing with aqueous saturated sodium chloride
- dry with materialAfter drying over anhydrous sodium sulfate and subsequent concentration under a reduced pressure
- customthe residue was purified by silica gel column chromatography
출처 및 근거
- ORD 기록
- ord-f386f690384a4225b083ba4e5a95032f
- 출처 데이터셋
- uspto-grants-2014_01
- 특허 번호
- US08629126B2
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