Trifluoroacetic acid → 1-{2-[6-(4-Cyclobutylpiperazin-1-yl)pyrimidin-4-yl]-3-oxo-2,3-dihydro-1H-pyrazol-4-yl}-1H-imidazole-4-carbonitrile

HRID 562462노트

반응식

HRID 562462 반응식
FC(F)(F)C(O)=O.C[N:9]([CH:11]=[C:12]([N:18]1[CH:22]=[C:21]([C:23]#[N:24])[N:20]=[CH:19]1)[C:13]([O:15]CC)=O)C.[CH:25]1([N:29]2[CH2:34][CH2:33][N:32]([C:35]3[CH:40]=[C:39]([NH:41]N)[N:38]=[CH:37][N:36]=3)[CH2:31][CH2:30]2)[CH2:28][CH2:27][CH2:26]1>C(OCC)(=O)C>[CH:25]1([N:29]2[CH2:34][CH2:33][N:32]([C:35]3[N:36]=[CH:37][N:38]=[C:39]([N:41]4[C:13](=[O:15])[C:12]([N:18]5[CH:22]=[C:21]([C:23]#[N:24])[N:20]=[CH:19]5)=[CH:11][NH:9]4)[CH:40]=3)[CH2:31][CH2:30]2)[CH2:26][CH2:27][CH2:28]1

참가 물질

5

반응물 3

HCID 6422Trifluoroacetic acidHCID 462211044-(4-Cyclobutylpiperazin-1-yl)-6-hydrazinopyrimidineHCID 66726020Ethyl 3-(N,N-dimethylamino)-2-(4-cyano-1H-imidazol-1-yl)acrylate

생성물 1

HCID 444646071-{2-[6-(4-Cyclobutylpiperazin-1-yl)pyrimidin-4-yl]-3-oxo-2,3-dihydro-1H-pyrazol-4-yl}-1H-imidazole-4-carbonitrile

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매

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온도
100 °C

실험 절차

16 μl (23 mg, 0.2 mmol) of trifluoroacetic acid are added to a mixture of 236 mg (1.0 mmol) of the compound from Example 6A and 250 mg (1.0 mmol) of the compound from Example 9A in 4 ml of ethyl acetate, and the mixture is stirred at 100° C. for 20 h. The reaction mixture is concentrated under reduced pressure, more ethyl acetate and trifluoroacetic acid (the same amounts as above) are added and the mixture is stirred at 100° C. for 3 d. The reaction mixture is cooled to RT, and the precipitated solid is filtered off and washed with diethyl ether. The residue is suspended in 2 ml of water, dissolved by adding aqueous 1 N sodium hydroxide solution (pH=9-10) and purified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient). Yield: 219 mg (56% of theory)

후처리

  1. concentrationThe reaction mixture is concentrated under reduced pressure, more ethyl acetate and trifluoroacetic acid (the same amounts as above)
  2. additionare added
  3. stirringthe mixture is stirred at 100° C. for 3 d
  4. temperatureThe reaction mixture is cooled to RT
  5. filtrationthe precipitated solid is filtered off
  6. washwashed with diethyl ether
  7. dissolutiondissolved
  8. additionby adding aqueous 1 N sodium hydroxide solution (pH=9-10)
  9. custompurified by preparative HPLC (RP18 column; mobile phase: acetonitrile/water gradient)

출처 및 근거

ORD 기록
ord-4edd7b9b6f484316b028239c5b8c8a8f
출처 데이터셋
uspto-grants-2011_11
특허 번호
US08067407B2

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