Triethylamine → 2-(p-Chlorophenyl)-4-phenyl-5-(trifluoromethyl)-3-[(trifluoromethyl)sulfonyl]pyrrole

HRID 1464679노트

반응식

HRID 1464679 반응식
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2C(=O)O[CH:10]([C:14]([F:17])([F:16])[F:15])[N:9]=2)=[CH:4][CH:3]=1.FC(F)(F)S([C:23]([S:31]([C:34]([F:37])([F:36])[F:35])(=[O:33])=[O:32])=[CH:24][C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1)(=O)=O.C(N(CC)CC)C>CN(C)C=O.C(OCC)(=O)C.O>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[NH:9][C:10]([C:14]([F:15])([F:16])[F:17])=[C:24]([C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)[C:23]=2[S:31]([C:34]([F:35])([F:36])[F:37])(=[O:32])=[O:33])=[CH:6][CH:7]=1

참가 물질

6

반응물 3

HCID 8471TriethylamineHCID 110652915(2H)-Oxazolone, 4-(4-chlorophenyl)-2-(trifluoromethyl)-HCID 18930436[2,2-Bis(trifluoromethanesulfonyl)ethenyl]benzene

생성물 1

HCID 189304082-(p-Chlorophenyl)-4-phenyl-5-(trifluoromethyl)-3-[(trifluoromethyl)sulfonyl]pyrrole

시약·촉매·용매 2

HCID 6228Dimethylformamide용매HCID 22728543Water ethylacetate용매

실험 절차

A solution of 4-(p-chlorophenyl)-2-(trifluoromethyl)-3-oxazolin-5-one (1.0 g, 3.8 mmol) and β,β-bis[(trifluoromethyl)sulfonyl]styrene (1.4 g, 3.8 mmol) in dimethylformamide is stirred for two hours at 110° C., treated with triethylamine (0.38 g, 3.8 mmol), stirred for several hours at reflux and diluted with an ethyl acetate/water mixture. The organic phase is separated, washed with water and dilute hydrochloric acid, dried over anhudrous magnesium sulfate and concentrated in vacuo to obtain a residue. Chromatography of the residue using silica gel and a 1:10 ethyl acetate/hexanes solution gives the title product as an amber oil which is identified by 1HNMR and 13CNMR spectral analyses.

후처리

  1. temperatureat reflux
  2. customThe organic phase is separated
  3. washwashed with water and dilute hydrochloric acid
  4. dry with materialdried over anhudrous magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customto obtain a residue

출처 및 근거

ORD 기록
ord-0ff990bb257d4768953eec820ad89491
출처 데이터셋
uspto-grants-1994_04
특허 번호
US05306827

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