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Dimethylformamide → 3-chloro-5-[(5-chloro-1H-indazol-4-yl)oxy]benzonitrile

HRID 505504
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HRID 505504 반응식
Br[C:2]1[CH:3]=[C:4]([CH:16]=[C:17]([Cl:19])[CH:18]=1)[O:5][C:6]1[C:14]([Cl:15])=[CH:13][CH:12]=[C:11]2[C:7]=1[CH:8]=[N:9][NH:10]2.[CH3:20][N:21](C=O)C>[C-]#N.[Zn+2].[C-]#N>[Cl:19][C:17]1[CH:18]=[C:2]([CH:3]=[C:4]([O:5][C:6]2[C:14]([Cl:15])=[CH:13][CH:12]=[C:11]3[C:7]=2[CH:8]=[N:9][NH:10]3)[CH:16]=1)[C:20]#[N:21]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6228DimethylformamideHCID 568336424-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazole

생성물 1

HCID 568336433-chloro-5-[(5-chloro-1H-indazol-4-yl)oxy]benzonitrile

시약·촉매·용매 1

HCID 11186Zinc cyanide (Zn(CN)2)촉매

반응 조건

온도
90 °C

실험 절차

To a suspension of 4-(3-bromo-5-chlorophenoxy)-5-chloro-1H-indazole (40 g, 112 mmol) and zinc cyanide (15.74 g, 134 mmol) in DMF (400 mL) was added palladium tetrakis triphenylphosphine (38.7 g, 33.5 mmol) and heated to 90° C. for 1 hour. After this time, the reaction was cooled to room temperature and partitioned between saturated aq. NH4Cl (500 mL), water (500 mL) and EtOAc (2×1000 mL). The combined extracts were dried over MgSO4, absorbed onto silica gel (200 g) and the solvent removed in vacuo. This solid was purified on a silica gel (1000 g) column (0-10% EtOAc/CH2Cl2) to give the title compound as a white solid. LRMS (M+1)=303.9

후처리

  1. temperatureAfter this time, the reaction was cooled to room temperature
  2. custompartitioned between saturated aq. NH4Cl (500 mL), water (500 mL) and EtOAc (2×1000 mL)
  3. dry with materialThe combined extracts were dried over MgSO4
  4. customabsorbed onto silica gel (200 g)
  5. customthe solvent removed in vacuo
  6. customThis solid was purified on a silica gel (1000 g) column (0-10% EtOAc/CH2Cl2)

출처 및 근거

ORD 기록
ord-43a9e2f84f874303ae3a5ec582a6c1ae
출처 데이터셋
uspto-grants-2010_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07781454B2

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