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Potassium Hydroxide → HCID 21226463, 화합물

HRID 583051
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HRID 583051 반응식
[OH-].[K+].[Cl:3][C:4]1[C:5]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([N:21](S(C)(=O)=O)[S:22]([CH3:25])(=[O:24])=[O:23])[CH:15]=2)=[N:6][N:7]([CH3:13])[C:8]=1[O:9][CH:10]([F:12])[F:11]>O.CO>[Cl:3][C:4]1[C:5]([C:14]2[CH:19]=[CH:18][C:17]([Cl:20])=[C:16]([NH:21][S:22]([CH3:25])(=[O:23])=[O:24])[CH:15]=2)=[N:6][N:7]([CH3:13])[C:8]=1[O:9][CH:10]([F:11])[F:12]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 14797Potassium HydroxideHCID 15220191HCID 15220191, 화합물

생성물 1

HCID 21226463HCID 21226463, 화합물수율 78.8%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water용매

실험 절차

0.3 g (4.7 mmol) of potassium hydroxide (dissolved in a little water) was added to a solution of 0.9 g (2.3 mmol) of 4-chloro-3-(4-chloro-3-[di-(methylsulfonyl)-amino]-phenyl)-5-difluoromethoxy-1-methyl-1H-pyrazole in 30 ml of methanol. The mixture was stirred at room temperature for 18 hours and then concentrated. The residue was taken up in 1N hydrochloric acid and then extracted with ethyl acetate. Drying of the organic phase with magnesium sulfate followed by concentration gave 0.7 g of the target product.

후처리

  1. concentrationconcentrated
  2. extractionextracted with ethyl acetate
  3. dry with materialDrying of the organic phase with magnesium sulfate
  4. concentrationfollowed by concentration

출처 및 근거

ORD 기록
ord-876060c4bdb340ac8ee827b2151cdd8c
출처 데이터셋
uspto-grants-1999_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05928999

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