5-{4-(Imidazo[1,2-a]pyridin-2-ylmethoxy)benzyl}-3-triphenylmethylthiazolidine-2,4-dione → 5-{4-(Imidazo[1,2-a]pyridin-2-ylmethoxy)benzyl}thiazolidine-2,4-dione

HRID 1601767노트

반응식

HRID 1601767 반응식
[N:1]1[C:2]([CH2:10][O:11][C:12]2[CH:44]=[CH:43][C:15]([CH2:16][CH:17]3[S:21][C:20](=[O:22])[N:19](C(C4C=CC=CC=4)(C4C=CC=CC=4)C4C=CC=CC=4)[C:18]3=[O:42])=[CH:14][CH:13]=2)=[CH:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12>FC(F)(F)C(O)=O>[N:1]1[C:2]([CH2:10][O:11][C:12]2[CH:13]=[CH:14][C:15]([CH2:16][CH:17]3[S:21][C:20](=[O:22])[NH:19][C:18]3=[O:42])=[CH:43][CH:44]=2)=[CH:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12

참가 물질

3

실험 절차

A procedure similar to that described in Example 1 was repeated, except that 3.0 g of 5-{4-(imidazo[1,2-a]pyridin-2-ylmethoxy) benzyl} -3-triphenylmethylthiazolidine-2,4-dione (prepared as described in Preparation 21) were reacted with 30 ml of trifluoroacetic acid for 1 hour. At the end of this time, the reaction mixture was freed from trifluoroacetic acid by distillation under reduced pressure. An aqueous solution of potassium carbonate and ethyl acetate were added to the residue, and the resulting precipitated insoluble material was collected by filtration, dried over anhydrous sodium sulfate and recrystallized from ethanol, to give 0.8 g of the title compound, melting at 197-202° C.

후처리

  1. distillationAt the end of this time, the reaction mixture was freed from trifluoroacetic acid by distillation under reduced pressure
  2. additionAn aqueous solution of potassium carbonate and ethyl acetate were added to the residue
  3. customthe resulting precipitated insoluble material
  4. filtrationwas collected by filtration
  5. dry with materialdried over anhydrous sodium sulfate
  6. customrecrystallized from ethanol

출처 및 근거

ORD 기록
ord-19150eec487849aaa44d533d19f0e2cd
출처 데이터셋
uspto-grants-1999_11
특허 번호
US05977365

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