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Sodium Hydroxide → HCID 18326251, 화합물

HRID 1250439
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HRID 1250439 반응식
[Cl:1][C:2]1[C:7]([C:8]([O:10]CC)=[O:9])=[CH:6][C:5]([C:13]2[C:17]([CH3:18])=[C:16]([C:19]#[N:20])[N:15]([CH3:21])[N:14]=2)=[C:4]([F:22])[CH:3]=1.[OH-].[Na+]>O1CCOCC1>[Cl:1][C:2]1[C:7]([C:8]([OH:10])=[O:9])=[CH:6][C:5]([C:13]2[C:17]([CH3:18])=[C:16]([C:19]#[N:20])[N:15]([CH3:21])[N:14]=2)=[C:4]([F:22])[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 18326242HCID 18326242, 화합물

생성물 1

HCID 18326251HCID 18326251, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

3.1 g of 3-(4-chloro-2-fluoro-5-carbethoxyphenyl)-4-methyl-5-cyano-1-methyl-[1H]-pyrazole (Example H13) are dissolved in 22 ml of dioxane, and 10 ml of 2N aqueous sodium hydroxide solution are added dropwise at 22° C. The mixture is stirred until the reaction is complete, the solvent is evaporated, the resulting residue is dissolved in water and the solution is brought to pH 1using hydrochloric acid. The precipitate formed is filtered off and dried. This gives the desired product in a yield of 2.63 g (89.8% of theory).

후처리

  1. customthe solvent is evaporated
  2. dissolutionthe resulting residue is dissolved in water
  3. customThe precipitate formed
  4. filtrationis filtered off
  5. customdried

출처 및 근거

ORD 기록
ord-6b603f1176a54d378053503ac41a7656
출처 데이터셋
uspto-grants-2002_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06339046B1

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