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Water → 6-Ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid

HRID 2095856
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인쇄 미리보기

반응식

HRID 2095856 반응식
[CH2:1]([C:3]1[N:8]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[C:7](=[O:16])[C:6]([C:17]#N)=[CH:5][CH:4]=1)[CH3:2].[OH2:19].[OH-:20].[Na+]>S(=O)(=O)(O)O>[CH2:1]([C:3]1[N:8]([C:9]2[CH:14]=[CH:13][C:12]([F:15])=[CH:11][CH:10]=2)[C:7](=[O:16])[C:6]([C:17]([OH:20])=[O:19])=[CH:5][CH:4]=1)[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 669688016-Ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile

생성물 1

HCID 581586366-Ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carboxylic acid수율 78%

시약·촉매·용매 1

HCID 1118Sulfuric Acid용매

실험 절차

A solution of 6-ethyl-1-(4-fluorophenyl)-2-oxo-1,2-dihydropyridine-3-carbonitrile (410 mg, 1.69 mmol) in conc. sulfuric acid (2 mL)/water (2 mL) was stirred at 120° C. for 17 hr. The reaction solution was allowed to cool to room temperature, 6N aqueous sodium hydroxide solution was added, and the aqueous layer was washed with ethyl acetate. 1N Hydrochloric acid was added to the aqueous layer, and the precipitate was collected by filtration and washed with water to give the title compound (345 mg, 78%) as a white solid.

후처리

  1. washthe aqueous layer was washed with ethyl acetate
  2. addition1N Hydrochloric acid was added to the aqueous layer
  3. filtrationthe precipitate was collected by filtration
  4. washwashed with water

출처 및 근거

ORD 기록
ord-9c27cc78d92b49f5b8c9fa6e908c254b
출처 데이터셋
uspto-grants-2013_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08445509B2

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