Triethylamine → N-(4-Benzoyl-2-cyanophenyl)-3,3,3,-trifluoro-2-hydroxy-2-methylpropanamide

HRID 1075388노트

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HRID 1075388 반응식
[F:1][C:2]([F:10])([F:9])[C:3]([OH:8])([CH3:7])[C:4](O)=[O:5].S(Cl)(Cl)=O.C(N(CC)CC)C.[C:22]([C:24]1[CH:25]=[C:26]([CH:35]=[CH:36][C:37]=1[NH2:38])[C:27]([C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)=[O:28])#[N:23]>C(Cl)Cl.O1CCCC1.C(OCC)C>[C:27]([C:26]1[CH:35]=[CH:36][C:37]([NH:38][C:4](=[O:5])[C:3]([OH:8])([CH3:7])[C:2]([F:10])([F:9])[F:1])=[C:24]([C:22]#[N:23])[CH:25]=1)(=[O:28])[C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1

참가 물질

8

실험 절차

To a stirred, cooled solution of 3,3,3-trifluoro-2-hydroxy-2-methylpropanoic acid (0.15 g) in methylene chloride (10 mL) was added thionyl chloride (0.12 g) and the mixture was stirred at reflux for 3 hours. The mixture was cooled to room temperature, triethylamine (0.11 g) added and the mixture stirred at reflux for 0.5 hour. The mixture was again cooled to room temperature, 3-cyano-4-aminobenzophenone (0.19 g) in tetrahydrofuran (2.5 mL) was added and the mixture stirred at reflux overnight. The solvent was evaporated and the residue partioned between ethyl acetate and 3N HCl. The organic layer was washed with water, dried and evaporated to yield a pale yellow oil. Chromatography (eluent methylene chloride then 2% ethyl ether in methylene chloride) gave the title compound (0.11 g) as a white solid; mp 202-204° C. Analysis for C18H13F3N2Ob .0.5 H2O: Calculated: C, 58.22; H, 3.80; N, 7,54; Found: C, 58.03; H, 3.57; N, 7.26.

후처리

  1. temperatureat reflux for 3 hours
  2. stirringthe mixture stirred
  3. temperatureat reflux for 0.5 hour
  4. temperatureThe mixture was again cooled to room temperature
  5. stirringthe mixture stirred
  6. temperatureat reflux overnight
  7. customThe solvent was evaporated
  8. washThe organic layer was washed with water
  9. customdried
  10. customevaporated
  11. customto yield a pale yellow oil

출처 및 근거

ORD 기록
ord-65a27ec7eabd46e2af7060b5d6555aa4
출처 데이터셋
uspto-grants-1999_05
특허 번호
US05900432

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