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N,N-dimethyl-4-nitrosoaniline → HCID 88465577, 화합물

HRID 1614492
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HRID 1614492 반응식
[Br-].[C:2]([C:4]1[CH:5]=[N:6][N:7]([C:16]2[C:21]([Cl:22])=[CH:20][C:19]([C:23]([F:26])([F:25])[F:24])=[CH:18][N:17]=2)[C:8]=1[CH2:9][N+]1C=CC=CC=1)#[N:3].[CH3:27][N:28]([CH3:37])[C:29]1[CH:34]=[CH:33][C:32]([N:35]=[O:36])=[CH:31][CH:30]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C.O>[CH3:27][N:28]([CH3:37])[C:29]1[CH:34]=[CH:33][C:32]([N+:35]([O-:36])=[CH:9][C:8]2[N:7]([C:16]3[C:21]([Cl:22])=[CH:20][C:19]([C:23]([F:26])([F:25])[F:24])=[CH:18][N:17]=3)[N:6]=[CH:5][C:4]=2[C:2]#[N:3])=[CH:31][CH:30]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 8749N,N-dimethyl-4-nitrosoanilineHCID 11430Potassium CarbonateHCID 19790766HCID 19790766, 화합물

생성물 1

HCID 88465577HCID 88465577, 화합물수율 87.4%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 962Water용매

실험 절차

To a stirred suspension of 9.0 grams (0.020 mole) of 1-[[4-cyano-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazol-5-yl]methyl]pyridinium bromide and 3.5 grams (0.023 mole) of N,N-dimethyl-4-nitrosoaniline in 95 mL of ethanol was added a solution of 16 grams (0.12 mole) of potassium carbonate in 59 mL of water. When the addition was complete, the reaction mixture was stirred at ambient temperature for four hours. After this time, the reaction mixture was filtered. The filter cake was washed in succession with water, ethanol, and diethyl ether, yielding 7.6 grams of N-[4-(dimethylamino)phenyl]-a-[4-cyano-1-(3-chloro-5-trifluoromethylpyridin-2-yl)-1H-pyrazol-5-yl]nitrone. The nmr spectrum was consistent with the proposed structure.

후처리

  1. additionWhen the addition
  2. filtrationAfter this time, the reaction mixture was filtered
  3. washThe filter cake was washed in succession with water, ethanol, and diethyl ether

출처 및 근거

ORD 기록
ord-ab03eee1af5b4ec88f8c80742e75487c
출처 데이터셋
uspto-grants-1993_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05198014

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