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Ammonia → 2,6-Difluoropyridine-3-carboxamide

HRID 50834
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HRID 50834 반응식
[F:1][C:2]1[N:10]=[C:9]([F:11])[CH:8]=[CH:7][C:3]=1[C:4](O)=[O:5].O=S(Cl)Cl.[NH3:16]>ClCCCl.CN(C=O)C>[F:1][C:2]1[N:10]=[C:9]([F:11])[CH:8]=[CH:7][C:3]=1[C:4]([NH2:16])=[O:5]
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참가 물질

6

반응물 3

HCID 222AmmoniaHCID 24386Thionyl ChlorideHCID 105830702,6-Difluoropyridine-3-carboxylic acid

생성물 1

HCID 105830482,6-Difluoropyridine-3-carboxamide수율 77,136.102%

시약·촉매·용매 2

HCID 6228Dimethylformamide촉매HCID 111,2-Dichloroethane용매

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온도
0 °C

실험 절차

A solution 2,6-difluoronicotinic acid (7.4 g, 0.046 mmol) and SOCl2 (20 mL) in 1,2-dichloroethane (60 mL) containing DMF (1 drop) is heated under reflux for 4 h, then concentrated to dryness under reduced pressure. The residue is dissolved in Et2O (100 mL), cooled to 0° C., and treated dropwise with concentrated ammonia (10.0 mL, 0.17 mmol). After 10 min the solution is washed with aqueous NaHCO3 and worked up to give 2,6-difluoronicotinamide (5.61 g, 76%). 1H NMR (CDCl3) a 8.70 (1H, dd, J=9.6, 8.3 Hz), 7.00 (1H, ddd, J=8.3, 2.9, 1.1 Hz), 6.71, 6.55 (1H, 1H, 2 brs)

후처리

  1. temperatureis heated
  2. temperatureunder reflux for 4 h
  3. concentrationconcentrated to dryness under reduced pressure
  4. dissolutionThe residue is dissolved in Et2O (100 mL)
  5. washAfter 10 min the solution is washed with aqueous NaHCO3

출처 및 근거

ORD 기록
ord-24264ffa5dd743e5b4dd3cbc634fc8a8
출처 데이터셋
uspto-grants-2004_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06713484B2

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