Triphenylphosphine → HCID 86757788, 화합물

HRID 1699738노트

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HRID 1699738 반응식
C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1.[F:20][C:21]([F:35])([F:34])[C:22]([NH:24][CH2:25][CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[C:29]([OH:33])[CH:28]=1)=[O:23].[CH3:36][O:37][C:38](=[O:55])[C:39]1[CH:44]=[C:43]([CH2:45]O)[CH:42]=[C:41]([C:47]2[CH:52]=[CH:51][CH:50]=[C:49]([C:53]#[N:54])[CH:48]=2)[CH:40]=1.[Cl-].[NH4+]>CCOC(/N=N/C(OCC)=O)=O>[CH3:36][O:37][C:38](=[O:55])[C:39]1[CH:44]=[C:43]([CH2:45][O:33][C:29]2[CH:30]=[CH:31][CH:32]=[C:27]([CH2:26][CH2:25][NH:24][C:22](=[O:23])[C:21]([F:34])([F:35])[F:20])[CH:28]=2)[CH:42]=[C:41]([C:47]2[CH:52]=[CH:51][CH:50]=[C:49]([C:53]#[N:54])[CH:48]=2)[CH:40]=1

참가 물질

6

실험 절차

110 mg of triphenylphosphine was dissolved in 5 ml of N-methylphosphine in the atmosphere of nitrogen, and 178 μl of DEAD was dropwisely dropped on the solution at 0° C. The obtained solution was mixed with 61 mg of (2,2,2-trifluoro-N-(2-(3-hydroxyphenyl)ethyl)ethanamide and 70 mg of 3-(3-cyanophenyl)-5-(hydroxymethyl)benzoic acid methyl ester, stirred at room temperature overnight and then poured on an aqueous solution of ammonium chloride to stop the reaction. The solution was extracted with ethyl acetate, and the obtained organic layer was dried. The solvent was distilled away, and the residue was purified by silica gel chromatography to obtain 79 mg (62.5%) of the title compound. Colorless solid.

후처리

  1. additionwas dropwisely dropped on the solution at 0° C
  2. customthe reaction
  3. extractionThe solution was extracted with ethyl acetate
  4. customthe obtained organic layer was dried
  5. distillationThe solvent was distilled away
  6. customthe residue was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-ee51d465add44f8091b2ac1b944bf328
출처 데이터셋
uspto-grants-2002_02
특허 번호
US06348478B1

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