Trifluoroacetic acid → HCID 178506540, 화합물

HRID 910243노트

반응식

HRID 910243 반응식
[I:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([C:10]3[CH:15]=[CH:14][C:13]([C:16]4[CH:20]=[CH:19][N:18](C(OC(C)(C)C)=O)[N:17]=4)=[CH:12][CH:11]=3)=[N:7][C:6]=2[CH:28]=1.FC(F)(F)C(O)=O>C(Cl)(Cl)Cl>[I:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([C:10]3[CH:11]=[CH:12][C:13]([C:16]4[CH:20]=[CH:19][NH:18][N:17]=4)=[CH:14][CH:15]=3)=[N:7][C:6]=2[CH:28]=1

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 67405262HCID 67405262, 화합물

생성물 1

HCID 178506540HCID 178506540, 화합물수율 84.5%

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

Subsequently, tert-butyl 3-[4-(5-iodo-1,3-benzoxazol-2-yl)phenyl]-1H-1-pyrazolecarboxylate (14.6 mg) was dissolved in chloroform (500 μL), and trifluoroacetic acid (231 μL) was added to the solution, followed by stirring at room temperature for 1 hour. The reaction mixture was concentrated under reduced pressure, followed by drying. The thus-obtained white solid was dissolved in chloroform, and the solution was washed sequentially with 1N aqueous sodium hydroxide, water, and saturated saline, followed by drying over magnesium sulfate. The solvent was evaporated under reduce pressure, and the solid was recovered through filtration by use of isopropyl ether, followed by drying under reduced pressure, to thereby yield the title compound (9.8 mg).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customby drying
  3. dissolutionThe thus-obtained white solid was dissolved in chloroform
  4. washthe solution was washed sequentially with 1N aqueous sodium hydroxide, water, and saturated saline
  5. dry with materialby drying over magnesium sulfate
  6. customThe solvent was evaporated
  7. filtrationthe solid was recovered through filtration by use of isopropyl ether
  8. customby drying under reduced pressure

출처 및 근거

ORD 기록
ord-cb9f05a5b750475c8f67e37817362ea1
출처 데이터셋
uspto-grants-2011_09
특허 번호
US08022075B2

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