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Sodium Hydroxide → HCID 14369785, 화합물

HRID 1381892
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HRID 1381892 반응식
[CH3:1][O:2][C:3]1([O:17]C)[C:8](=O)[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=2)[S:4]1.[OH-].[Na+]>Cl>[CH3:10][C:6]1[N:7]=[C:8]([C:3]([O:2][CH3:1])=[O:17])[S:4][C:5]=1[C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 139360292,2-Dimethoxy-5-methyl-6-(pyridin-4-yl)-2H-1,4-thiazin-3(4H)-one

생성물 1

HCID 14369785HCID 14369785, 화합물수율 90%

시약·촉매·용매 1

HCID 313Hydrochloric Acid용매

실험 절차

2,2-Dimethoxy-5-methyl-6-(4-pyridinyl)-2H-1,4-thiazin-3(4H)-one (200 mg) was dissolved in 2N hydrochloric acid (2 ml), and the mixture was allowed to stand at room temperature for 30 minutes. Then, the solution was made alkaline by addition of 2N aqueous sodium hydroxide under ice-cooling, and the resulting precipitates were collected by filtration. The precipitates were washed with water, air-dried, and was recrystallized from benzene-petroleum ether to give methyl 4-methyl-5-(4-pyridinyl)-thiazole-2-carboxylate (158 mg, yield 90%) as colorless needles.

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후처리

  1. temperaturecooling
  2. customthe resulting precipitates
  3. filtrationwere collected by filtration
  4. washThe precipitates were washed with water
  5. customair-dried
  6. customwas recrystallized from benzene-petroleum ether

출처 및 근거

ORD 기록
ord-595081867cc74dc29e6e40faaf3e0e51
출처 데이터셋
uspto-grants-1989_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04804668

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