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Potassium Carbonate → 2-(4-(1-(4-methoxybenzyl)-3-(1-methylpiperidin-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-4-yloxy)-3-fluorophenylamino)-N-(4-fluorophenyl)nicotinamide

HRID 2241396
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HRID 2241396 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][CH:5]([NH2:8])[CH2:4][CH2:3]1.C([O-])([O-])=O.[K+].[K+].N1CCC[C@H]1C(O)=O.[CH3:23][O:24][C:25]1[CH:66]=[CH:65][C:28]([CH2:29][N:30]2[C:34]3=[N:35][CH:36]=[CH:37][C:38]([O:39][C:40]4[CH:45]=[CH:44][C:43]([NH:46][C:47]5[N:62]=[CH:61][CH:60]=[CH:59][C:48]=5[C:49]([NH:51][C:52]5[CH:57]=[CH:56][C:55]([F:58])=[CH:54][CH:53]=5)=[O:50])=[CH:42][C:41]=4[F:63])=[C:33]3[C:32](I)=[N:31]2)=[CH:27][CH:26]=1>CS(C)=O.O.C(Cl)Cl>[CH3:23][O:24][C:25]1[CH:26]=[CH:27][C:28]([CH2:29][N:30]2[C:34]3=[N:35][CH:36]=[CH:37][C:38]([O:39][C:40]4[CH:45]=[CH:44][C:43]([NH:46][C:47]5[N:62]=[CH:61][CH:60]=[CH:59][C:48]=5[C:49]([NH:51][C:52]5[CH:57]=[CH:56][C:55]([F:58])=[CH:54][CH:53]=5)=[O:50])=[CH:42][C:41]=4[F:63])=[C:33]3[C:32]([NH:8][CH:5]3[CH2:6][CH2:7][N:2]([CH3:1])[CH2:3][CH2:4]3)=[N:31]2)=[CH:65][CH:66]=1
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참가 물질

8

반응물 4

HCID 11430Potassium CarbonateHCID 145742L-ProlineHCID 27375314-Amino-1-methylpiperidineHCID 672218582-(4-(1-(4-methoxybenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridin-4-yloxy)-3-fluorophenylamino)-N-(4-fluorophenyl)nicotinamide

생성물 1

HCID 685161762-(4-(1-(4-methoxybenzyl)-3-(1-methylpiperidin-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-4-yloxy)-3-fluorophenylamino)-N-(4-fluorophenyl)nicotinamide
수율 11.7%

시약·촉매·용매 3

HCID 679Dimethyl Sulfoxide용매2회HCID 962Water용매HCID 6344Dichloromethane용매

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온도
100 °C

실험 절차

A 25 mL round-bottomed flask was charged with Cu(I)I (0.0108 g, 0.0568 mmol), 1-methylpiperidin-4-amine (0.0973 g, 0.852 mmol), K2CO3 (0.196 g, 1.42 mmol), L-Proline (0.0131 g, 0.114 mmol) and DMSO (2.5 mL). The reaction mixture was stirred for 5 minutes and 2-(4-(1-(4-methoxybenzyl)-3-iodo-1H-pyrazolo[3,4-b]pyridin-4-yloxy)-3-fluorophenylamino)-N-(4-fluorophenyl)nicotinamide (0.200 g, 0.284 mmol) in DMSO (2.5 mL) was added. The reaction mixture was heated to 100° C. for 18 hours. The reaction mixture was cooled to ambient temperature and DCM and water (10 mL) were added. The organic layer washed with brine, dried over sodium sulfate, filtered and concentrated. The crude material was purified by silica gel chromatography, eluting with EtOAc to provide the product (23 mg, 11%). LRMS M−1 (691.2) observed.

후처리

  1. temperatureThe reaction mixture was cooled to ambient temperature
  2. washThe organic layer washed with brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude material was purified by silica gel chromatography
  7. washeluting with EtOAc

출처 및 근거

ORD 기록
ord-00f80b82dfec43baad7501069cb573f0
출처 데이터셋
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07723330B2

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