Water → Convergence

HRID 418294노트

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HRID 418294 반응식
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:8]=[CH:7][C:6]([S:9]([N:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)(=[O:11])=[O:10])=[CH:5][CH:4]=1.[N:20]1[N:24]2[CH:25]=[CH:26][CH:27]=[N:28][C:23]2=[C:22]([C:29](O)=[O:30])[CH:21]=1.C1C=CC2N(O)N=NC=2C=1.O.CN(C(ON1N=NC2C=CC=CC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C>CN(C=O)C>[F:19][C:2]([F:1])([F:18])[C:3]1[CH:4]=[CH:5][C:6]([S:9]([N:12]2[CH2:17][CH2:16][N:15]([C:29]([C:22]3[CH:21]=[N:20][N:24]4[CH:25]=[CH:26][CH:27]=[N:28][C:23]=34)=[O:30])[CH2:14][CH2:13]2)(=[O:10])=[O:11])=[CH:7][CH:8]=1

참가 물질

8

실험 절차

To a solution of 1-{[4-(trifluoromethyl)phenyl]sulfonyl}piperazine (may be prepared as described in Description 1) (200 mg, 0.680 mmol) in DMF (5 ml) was added pyrazolo[1,5-a]pyrimidine-3-carboxylic acid (111 mg, 0.680 mmol), HOBT.H2O (104 mg, 0.680 mmol) and HBTU (258 mg, 0.680 mmol). Finally DIPEA (0.356 ml, 2.039 mmol) was added and the reaction mixture was stirred at rt for 20 hours. Solvent was removed by evaporation, the crude partitioned between DCM (50 ml) and saturated aq. sodium bicarbonate (50 ml), the DCM layer collected, dried (hydrophobic frit) and evaporated. MDAP purification yielded the title compound (317 mg) as an off-white solid.

후처리

  1. customSolvent was removed by evaporation
  2. customthe crude partitioned between DCM (50 ml) and saturated aq. sodium bicarbonate (50 ml)
  3. customthe DCM layer collected
  4. customdried (hydrophobic frit)
  5. customevaporated
  6. customMDAP purification

출처 및 근거

ORD 기록
ord-48aa982af32e44d6ad25a834957fe306
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08093249B2

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