Water → HCID 16643583, 화합물

HRID 423103노트

반응식

HRID 423103 반응식
CO/[N:3]=[C:4](\[C:11]1[CH:16]=[CH:15][C:14]([Cl:17])=[CH:13][CH:12]=1)/[CH2:5][N:6]1[CH:10]=[CH:9][CH:8]=[N:7]1.O.[OH-].[Na+].C(OCC)C>C1COCC1>[Cl:17][C:14]1[CH:15]=[CH:16][C:11]([CH:4]([NH2:3])[CH2:5][N:6]2[CH:10]=[CH:9][CH:8]=[N:7]2)=[CH:12][CH:13]=1

참가 물질

6

반응물 4

HCID 962WaterHCID 3283Diethyl EtherHCID 14798Sodium HydroxideHCID 57750295(E)-1-(4-chlorophenyl)-N-methoxy-2-pyrazol-1-ylethanimine3회

생성물 1

HCID 16643583HCID 16643583, 화합물수율 55%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Borane tetrahydrofuran complex (15.00 mL, 15.00 mmol) was added to a stirred solution of (Z) and (E)-1-(4-chlorophenyl)-2-(1H-pyrazol-1-yl)ethanone O-methyl oxime (Intermediate 91) (0.749 g, 3 mmol) dissolved in THF (30 mL) at room temperature under argon. The resulting solution was stirred under reflux for 3 hours. The mixture was cooled in an ice/water bath and water (25 ml) was carefully added followed by 20% NaOH (25 ml). The resulting biphasic mixture was refluxed overnight with vigorous magnetic stirring and allowed to cool. Diethyl ether was added and the layers were separated. The organic layer was further extracted with diethyl ether dried over MgSO4, filtered and evaporated to give the crude product (741 mg, 55%). This was used directly in the following reaction.

후처리

  1. temperatureunder reflux for 3 hours
  2. temperatureThe mixture was cooled in an ice/water bath
  3. temperatureThe resulting biphasic mixture was refluxed overnight with vigorous
  4. stirringmagnetic stirring
  5. temperatureto cool
  6. customthe layers were separated
  7. extractionThe organic layer was further extracted with diethyl ether
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. customevaporated

출처 및 근거

ORD 기록
ord-b8970c45f9ad400aa664dea73f5cbec4
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08101623B2

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