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Acetic Acid → HCID 57758602, 화합물

HRID 229402
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HRID 229402 반응식
C([O:3][C:4]([C:6]1[C:7]([NH:21][NH2:22])=[N:8][C:9]([O:12][C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=2[F:20])=[N:10][CH:11]=1)=O)C.CC[O-].[Na+].CC(O)=O.O>CCO>[F:20][C:14]1[CH:15]=[C:16]([F:19])[CH:17]=[CH:18][C:13]=1[O:12][C:9]1[N:8]=[C:7]2[NH:21][NH:22][C:4](=[O:3])[C:6]2=[CH:11][N:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 176Acetic AcidHCID 962WaterHCID 2723922Sodium ethoxideHCID 57758598HCID 57758598, 화합물

생성물 1

HCID 57758602HCID 57758602, 화합물수율 78.9%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A solution of 2-(2,4-difluoro-phenoxy)-4-hydrazino-pyrimidine-5-carboxylic acid ethyl ester (7.0 g) and NaOEt (21% in EtOH, 16.85 mL) in EtOH (56 mL) was heated to 55° C. for two hours. The reaction was cooled, and HOAc was added to adjust pH to around 5.0. Water was added until no more precipitation occurred, and the mixture was filtered. The precipitate was collected and dried under vacuum to give 6-(2,4-difluoro-phenoxy)-1,2-dihydro-pyrazolo[3,4-d]pyrimidin-3-one (4.7 g).

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후처리

  1. temperatureThe reaction was cooled
  2. filtrationthe mixture was filtered
  3. customThe precipitate was collected
  4. customdried under vacuum

출처 및 근거

ORD 기록
ord-72952922383843c691a430846a086e9b
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07563800B2

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