Citric Acid → 2-(4-methyl-1-piperidyl)-N-[[2-(trifluoromethyl)-1H-indol-5-yl]methyl]-pyrimidine-5-carboxamide

HRID 388394노트

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HRID 388394 반응식
CN(C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.[CH3:25][CH:26]1[CH2:31][CH2:30][N:29]([C:32]2[N:37]=[CH:36][C:35]([C:38]([OH:40])=O)=[CH:34][N:33]=2)[CH2:28][CH2:27]1.CCN(C(C)C)C(C)C.[F:50][C:51]([F:64])([F:63])[C:52]1[NH:53][C:54]2[C:59]([CH:60]=1)=[CH:58][C:57]([CH2:61][NH2:62])=[CH:56][CH:55]=2.C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN(C=O)C>[CH3:25][CH:26]1[CH2:27][CH2:28][N:29]([C:32]2[N:33]=[CH:34][C:35]([C:38]([NH:62][CH2:61][C:57]3[CH:58]=[C:59]4[C:54](=[CH:55][CH:56]=3)[NH:53][C:52]([C:51]([F:64])([F:50])[F:63])=[CH:60]4)=[O:40])=[CH:36][N:37]=2)[CH2:30][CH2:31]1

참가 물질

7

실험 절차

To a stirred solution of HATU (34.4 mg, 0.090 mmol) in 1 ml DMF was added (2-(4-methyl-1-piperidinyl)-5-pyrimidinecarboxylic acid) (Matrix Scientific, 20 mg, 0.090 mmol) in 0.5 ml DMF, followed by DIPEA (0.016 ml, 0.090 mmol) and finally {[2-(trifluoromethyl)-1H-indol-5-yl]methyl}amine (Intermediate 4, 22.66 mg, 0.090 mmol) in 1 ml DMF. Stirring was continued for 16 hours. 1M citric acid solution (10 ml) was added and the mixture was then extracted with ethyl acetate (20 ml). The organic extract was then washed with 1M citric acid solution (10 ml), brine (10 ml), dried (MgSO4), filtered and evaporated to dryness. The resulting residues where then purified on the MDAP to dryness to give the title compound (19 mg);

후처리

  1. extractionthe mixture was then extracted with ethyl acetate (20 ml)
  2. extractionThe organic extract
  3. washwas then washed with 1M citric acid solution (10 ml), brine (10 ml)
  4. dry with materialdried (MgSO4)
  5. filtrationfiltered
  6. customevaporated to dryness
  7. customThe resulting residues where then purified on the MDAP to dryness

출처 및 근거

ORD 기록
ord-b3a424193d0047daabfbaef6aad04fa9
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08377941B2

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