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Sodium Hydroxide → (5-Methyl-2-pyridin-3-yl-1,3-oxazol-4-yl)acetic acid

HRID 2211978
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HRID 2211978 반응식
[OH-].[Li+].[CH3:3][C:4]1[O:8][C:7]([C:9]2[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=2)=[N:6][C:5]=1[CH2:15][C:16]([OH:18])=[O:17].[OH-].[Na+]>C(O)C>[CH3:3][C:4]1[O:8][C:7]([C:9]2[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=2)=[N:6][C:5]=1[CH2:15][C:16]([OH:18])=[O:17]
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참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 69584659(5-Methyl-2-pyridin-3-yl-1,3-oxazol4-yl)acetic acid lithium hydroxide

생성물 1

HCID 21962835(5-Methyl-2-pyridin-3-yl-1,3-oxazol-4-yl)acetic acid수율 425.4%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
22 °C

실험 절차

(5-Methyl-2-pyridin-3-yl-1,3-oxazol4-yl)acetic acid lithium hydroxide (12 mg) added. The mixture was stirred at 22° C. for 17 h and heated at 60° C. for 2 h. Ethanol (3 ml) and 2N aqueous sodium hydroxide (1 ml) were added, and stirring was continued at 22° C. for 2 h. The mixture was applied to a sulphonic acid ion exchange cartridge (10 g Isolute SCX) and eluted with methanol followed by 10% triethylamine in methanol. Evaporation of the triethylamine containing fraction gave the title compound as a gum (46 mg).

후처리

  1. temperatureheated at 60° C. for 2 h
  2. stirringstirring
  3. waitwas continued at 22° C. for 2 h
  4. washeluted with methanol
  5. customEvaporation of the triethylamine containing fraction

출처 및 근거

ORD 기록
ord-a7f46ab882a34366a3bd8509dbe0b5b8
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07101882B2

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