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Cesium carbonate → 5-chloro-2-(4-fluoro-2-methoxyphenoxy)-N-(2-oxo-1,2-dihydropyridin-4-yl)benzamide

HRID 2170435
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HRID 2170435 반응식
[C:1]([O-:4])([O-])=O.[Cs+].[Cs+].F[C:8]1[CH:23]=[CH:22][C:21]([Cl:24])=[CH:20][C:9]=1[C:10]([NH:12][C:13]1[CH:18]=[CH:17][NH:16][C:15](=[O:19])[CH:14]=1)=[O:11].[F:25][C:26]1[CH:31]=[CH:30][C:29]([OH:32])=[CH:28][C:27]=1OC>CN(C=O)C>[Cl:24][C:21]1[CH:22]=[CH:23][C:8]([O:32][C:29]2[CH:30]=[CH:31][C:26]([F:25])=[CH:27][C:28]=2[O:4][CH3:1])=[C:9]([CH:20]=1)[C:10]([NH:12][C:13]1[CH:18]=[CH:17][NH:16][C:15](=[O:19])[CH:14]=1)=[O:11]
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참가 물질

5

반응물 3

HCID 10796Cesium carbonateHCID 141189564-Fluoro-3-methoxyphenolHCID 867284695-chloro-2-fluoro-N-(2-oxo-1H-pyridin-4-yl)benzamide

생성물 1

HCID 783234265-chloro-2-(4-fluoro-2-methoxyphenoxy)-N-(2-oxo-1,2-dihydropyridin-4-yl)benzamide수율 30.3%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
100 °C

실험 절차

Cs2CO3 (879.9 mg, 2.7 mmol) was added to a solution of 2-fluoro-N-(2-oxo-1,2-dihydropyridin-4-yl)-5-chlorobenzamide (72.0 mg, 0.27 mmol) and 4-fluoro-3-methoxyphenol (307.7 μl, 2.7 mmol) in DMF (1 mL) and the reaction was stirred at 100° C. for 1 hour. The reaction was filtered and purified by reverse phase HPLC using a gradient of acetonitrile in water (10-99%) and HCl as a modifier to yield 5-chloro-2-(4-fluoro-2-methoxyphenoxy)-N-(2-oxo-1,2-dihydropyridin-4-yl)benzamide (70) (31.8 mg, 30%). ESI-MS m/z calc. 388.06. found 389.10 (M+1)+; Retention time: 1.52 minutes (3 minutes run).

후처리

  1. filtrationThe reaction was filtered
  2. custompurified by reverse phase HPLC

출처 및 근거

ORD 기록
ord-cefbe29afc894ae685db7f290da34783
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09051270B2

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