Piperidine, 1-(2-chloroethyl)-, hydrochloride → 3-({7-Chloro-1-[2-(piperidin-1-yl)ethyl]-1,4-dihydroquinolin-4-ylidene}amino)-5-{[2-(piperidin-1-yl)ethyl]amino}benzonitrile
반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:7]=[C:8]([N:10]=[C:11]2[C:20]3[C:15](=[CH:16][C:17]([Cl:21])=[CH:18][CH:19]=3)[N:14]([CH2:22][CH2:23][N:24]3[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]3)[CH:13]=[CH:12]2)[CH:9]=1)[C:5]#[N:6].Cl.Cl[CH2:32][CH2:33][N:34]1[CH2:39][CH2:38][CH2:37][CH2:36][CH2:35]1.CCN(C(C)C)C(C)C>CC(CC)CO>[Cl:21][C:17]1[CH:16]=[C:15]2[C:20]([C:11](=[N:10][C:8]3[CH:7]=[C:4]([CH:3]=[C:2]([NH:1][CH2:32][CH2:33][N:34]4[CH2:39][CH2:38][CH2:37][CH2:36][CH2:35]4)[CH:9]=3)[C:5]#[N:6])[CH:12]=[CH:13][N:14]2[CH2:22][CH2:23][N:24]2[CH2:29][CH2:28][CH2:27][CH2:26][CH2:25]2)=[CH:19][CH:18]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
3-amino-5-({7-chloro-1-[2-(piperidin-1-yl)ethyl]-1,4-dihydroquinolin-4-ylidene}amino)benzonitrile prepared from example 21 (132 mg, 0.32 mmol), 1-(2-chloroethyl)piperidine hydrochloride (182 mg, 3 eq) and DIEA (0.51 mL, 9.3 eq) were refluxed in 15 mL of 2-methylbutan-1-ol for 10 h. The reaction mixture was then evaporated and the residue and was purified by preparative thin-layer chromatography (DCM/MeOH/NH4OH//95/5/1) to yield expected compound as a yellow oil (28 mg, 17% yield). m/z (ESI) 517.5 [M+H]+.
후처리
- customThe reaction mixture was then evaporated
- customthe residue and was purified by preparative thin-layer chromatography (DCM/MeOH/NH4OH//95/5/1)
출처 및 근거
- ORD 기록
- ord-246d17e0bae44081a8e50011d83dff61
- 출처 데이터셋
- uspto-grants-2014_03
- 특허 번호
- US08680095B2
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