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Ammonium Chloride → [1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-3-(2-thienyl)-1H-pyrazol-4-yl]acetonitrile

HRID 350024
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HRID 350024 반응식
C1(C)C=CC(S([CH2:10][N+:11]#[C-])(=O)=O)=CC=1.CC(C)([O-])C.[K+].[CH3:20][C:21]1[O:25][C:24]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)=[N:23][C:22]=1[CH2:32][O:33][C:34]1[CH:52]=[CH:51][C:37]([CH2:38][N:39]2[CH:43]=[C:42]([CH:44]=O)[C:41]([C:46]3[S:47][CH:48]=[CH:49][CH:50]=3)=[N:40]2)=[CH:36][CH:35]=1.[Cl-].[NH4+]>C(COC)OC.CO>[CH3:20][C:21]1[O:25][C:24]([C:26]2[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=2)=[N:23][C:22]=1[CH2:32][O:33][C:34]1[CH:52]=[CH:51][C:37]([CH2:38][N:39]2[CH:43]=[C:42]([CH2:44][C:10]#[N:11])[C:41]([C:46]3[S:47][CH:48]=[CH:49][CH:50]=3)=[N:40]2)=[CH:36][CH:35]=1
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참가 물질

7

반응물 4

HCID 25517Ammonium ChlorideHCID 161915Tosylmethyl isocyanideHCID 230248961-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-3-(2-thienyl)-1H-pyrazole-4-carbaldehydeHCID 23665647Potassium tert-butoxide

생성물 1

HCID 69421547[1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-3-(2-thienyl)-1H-pyrazol-4-yl]acetonitrile수율 82.1%

시약·촉매·용매 2

HCID 887Methanol용매HCID 80711,2-Dimethoxyethane용매3회

실험 절차

A solution of p-toluenesulfonylmethylisocyanide (0.95 g) in dimethoxyethane (10 ml) was added to a mixture of potassium tert-butoxide (1.01 g) and dimethoxyethane (10 ml) at −78° C., and the mixture was stirred for 5 minutes. A solution of 1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-3-(2-thienyl)-1H-pyrazole-4-carbaldehyde (2.01 g) in dimethoxyethane (20 ml) was added to the mixture, and then stirred at the same temperature for 1 hour, and at room temperature for 1 hour. Methanol (40 ml) was added to the mixture, and reflux was conducted for 1 hour. After cooling, the reaction mixture was poured into saturated aqueous ammonium chloride solution, and extracted with ethyl acetate. The ethyl acetate layer was washed with saturated aqueous sodium chloride solution, dried (MgSO4), and concentrated. The residue was subjected to silica gel chromatography to obtain [1-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyl]-3-(2-thienyl)-1H-pyrazol-4-yl]acetonitrile (1.69 g, yield: 78%) as a colorless oily substance from the fraction eluted with ethyl acetate-hexane (1:3, volume ratio).

후처리

  1. stirringstirred at the same temperature for 1 hour
  2. waitat room temperature for 1 hour
  3. temperaturereflux
  4. waitwas conducted for 1 hour
  5. temperatureAfter cooling
  6. extractionextracted with ethyl acetate
  7. washThe ethyl acetate layer was washed with saturated aqueous sodium chloride solution
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated

출처 및 근거

ORD 기록
ord-6bd7ee6e00b64136bec2f2346936d748
출처 데이터셋
uspto-grants-2007_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07179823B1

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