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Sodium Hydroxide → HCID 23443407, 화합물

HRID 2119787
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HRID 2119787 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9](O)[CH:10]([C:14]3[C:19]([F:20])=[CH:18][CH:17]=[CH:16][C:15]=3[F:21])[N:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1.O=P(Cl)(Cl)[Cl:25].[OH-].[Na+]>O>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]([Cl:25])[CH:10]([C:14]3[C:19]([F:20])=[CH:18][CH:17]=[CH:16][C:15]=3[F:21])[N:11]=[CH:12][CH:13]=2)=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14798Sodium HydroxideHCID 24813Phosphorus oxychlorideHCID 234434054-(4-Bromophenyl)-2-(2,6-difluorophenyl)-3-hydroxypyrimidine

생성물 1

HCID 23443407HCID 23443407, 화합물

시약·촉매·용매 1

HCID 962Water용매

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온도
110 °C

실험 절차

23.2 g of 4-(4-bromophenyl)-2-(2,6-difluorophenyl)-3-hydroxypyrimidine and 100 ml of POCl3 are mixed and stirred for one hour at 110° C. The reaction mixture is slowly poured into a solution of 250 g of NaOH (solid) in water, and filtered. After dissolving the precipitate in ethyl acetate, drying with magnesium sulfate, filtering and concentrating, the title compound is obtained with a melting point of 146-148° C. (compound 3.354).

후처리

  1. filtrationfiltered
  2. dissolutionAfter dissolving the precipitate in ethyl acetate
  3. dry with materialdrying with magnesium sulfate
  4. filtrationfiltering
  5. concentrationconcentrating

출처 및 근거

ORD 기록
ord-9654a4740bbf47e991f4083f6edcc055
출처 데이터셋
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06686469B2

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