Potassium Carbonate → 1-(2,2-dimethoxyethyl)-7-fluoro-1,5-naphthyridin-2(1H)-one

HRID 1804721ノート

反応式

HRID 1804721 の反応式
[CH3:1][O:2][CH:3]([O:17][CH3:18])[CH2:4][N:5]1[C:14]2[C:9](=[N:10][CH:11]=[C:12]([F:15])[CH:13]=2)[CH2:8][CH2:7][C:6]1=[O:16].BrN1C(=O)CCC1=O.C(=O)([O-])[O-].[K+].[K+].[OH-].[Na+]>ClC1C=CC=CC=1.N(C(C)(CC(OC)(C)C)C#N)=NC(C)(CC(C)(OC)C)C#N.O>[CH3:18][O:17][CH:3]([O:2][CH3:1])[CH2:4][N:5]1[C:14]2[C:9](=[N:10][CH:11]=[C:12]([F:15])[CH:13]=2)[CH:8]=[CH:7][C:6]1=[O:16]

参加物

8

反応物 4

HCID 11430Potassium CarbonateHCID 14798Sodium HydroxideHCID 67184N-bromobutanimideHCID 595107361-(2,2-dimethoxyethyl)-7-fluoro-3,4-dihydro-1,5-naphthyridin-2(1H)-one

生成物 1

HCID 595107441-(2,2-dimethoxyethyl)-7-fluoro-1,5-naphthyridin-2(1H)-one収率 82.7%

試薬・触媒・溶媒 3

HCID 858672,2'-Azobis(2,4-dimethyl-4-methoxyvaleronitrile)触媒HCID 962Water溶媒HCID 7964Chlorobenzene溶媒

実験手順

To a suspension of 5.0 g of 1-(2,2-dimethoxyethyl)-7-fluoro-3,4-dihydro-1,5-naphthyridin-2(1H)-one, 5.3 g of N-bromosuccinimide and 3.0 g of potassium carbonate in 30 mL of chlorobenzene, 0.12 g of 2,2′-azobis(4-methoxy-2,4-dimethylvaleronitrile) was added three times hourly at 50 to 60° C. under a nitrogen atmosphere. After stirring the reaction mixture for 1 hour at the same temperature, 10 mL of water was added thereto, and the mixture was adjusted to pH 12.6 using a 20% sodium hydroxide solution. The organic layer was separated and washed with 15 mL of water. The aqueous layer was extracted with 15 mL of toluene. The organic layer and the extract were combined to evaporate the solvent under reduced pressure. To the obtained residue, 2 mL of chlorobenzene and 6 mL of cyclohexane were added, the mixture was stirred for 30 minutes under ice cooling, and the solid product was obtained by filtration and washed with cyclohexane to give 4.1 g of 1-(2,2-dimethoxyethyl)-7-fluoro-1,5-naphthyridin-2(1H)-one as a light yellow solid.

後処理

  1. additionwas added three times hourly at 50 to 60° C. under a nitrogen atmosphere
  2. additionwas added
  3. customThe organic layer was separated
  4. washwashed with 15 mL of water
  5. extractionThe aqueous layer was extracted with 15 mL of toluene
  6. customto evaporate the solvent under reduced pressure
  7. additionTo the obtained residue, 2 mL of chlorobenzene and 6 mL of cyclohexane were added
  8. customthe solid product was obtained by filtration
  9. washwashed with cyclohexane

出典と根拠

ORDレコード
ord-bb90db7725b24cfa9479b812a36e71eb
出典データセット
uspto-grants-2013_01
特許番号
US08354426B2

反応ノート

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