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Sodium hydride → 6-Chloro-2-(2,2-difluoro-ethoxy)-nicotinamide

HRID 1471587
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HRID 1471587 반응식
[F:1][CH:2]([F:5])[CH2:3][OH:4].[H-].[Na+].Cl[C:9]1[N:17]=[C:16]([Cl:18])[CH:15]=[CH:14][C:10]=1[C:11]([NH2:13])=[O:12]>COCCOC.CN(C)C=O.O>[Cl:18][C:16]1[CH:15]=[CH:14][C:10]([C:11]([NH2:13])=[O:12])=[C:9]([O:4][CH2:3][CH:2]([F:5])[F:1])[N:17]=1
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참가 물질

7

반응물 3

HCID 24758Sodium hydrideHCID 1361872,2-Difluoroethan-1-olHCID 221427782,6-Dichloropyridine-3-carboxamide

생성물 1

HCID 579690086-Chloro-2-(2,2-difluoro-ethoxy)-nicotinamide수율 97.5%

시약·촉매·용매 3

HCID 962Water용매HCID 6228Dimethylformamide용매
HCID 80711,2-Dimethoxyethane용매

실험 절차

2,2-Difluoroethanol (3.51 mL, 55.5 mmol) was added dropwise over 30 minutes to a suspension of NaH (2.22 g, 60% w/w dispersion in oil) in 1,2-dimethoxyethane (40.0 mL) at 14° C. and stirred for 1 hour. A portion of this solution (25 mL, 35 mmol) was added dropwise over 10 minutes to a solution of 2,6-dichloro-nicotinamide (5.30 g, 27.7 mmol) in dimethylformamide (40 mL) at 14° C. The resultant suspension was stirred for an additional 1 hour at 14° C., diluted with water (600 mL) and extracted with EtOAc (3×400 mL). The organic extracts were combined, dried over Na2SO4, filtered and concentrated to give title compound as a light orange solid (6.39 g, 97%). This was used without further purification.

후처리

  1. extractionextracted with EtOAc (3×400 mL)
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated

출처 및 근거

ORD 기록
ord-8ee9b7b8e7c24bbead2b870929f2be7f
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012431B2

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