Methyl iodide → 2-(4-((3-(4-Methoxypiperidin-1-yl)pyrazin-2-yl)oxy)piperidin-1-yl)quinoline

HRID 2207821노트

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HRID 2207821 반응식
[N:1]1[C:10]2[C:5](=[CH:6][CH:7]=[CH:8][CH:9]=2)[CH:4]=[CH:3][C:2]=1[N:11]1[CH2:16][CH2:15][CH:14]([O:17][C:18]2[C:19]([N:24]3[CH2:29][CH2:28][CH:27]([OH:30])[CH2:26][CH2:25]3)=[N:20][CH:21]=[CH:22][N:23]=2)[CH2:13][CH2:12]1.[C:31]([O-])([O-])=O.[Cs+].[Cs+].IC>C(#N)C>[CH3:31][O:30][CH:27]1[CH2:28][CH2:29][N:24]([C:19]2[C:18]([O:17][CH:14]3[CH2:13][CH2:12][N:11]([C:2]4[CH:3]=[CH:4][C:5]5[C:10](=[CH:9][CH:8]=[CH:7][CH:6]=5)[N:1]=4)[CH2:16][CH2:15]3)=[N:23][CH:22]=[CH:21][N:20]=2)[CH2:25][CH2:26]1

참가 물질

5

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온도
0 °C

실험 절차

To a solution of 1-(3-((1-(quinolin-2-yl)piperidin-4-yl)oxy)pyrazin-2-yl)piperidin-4-ol (see EXAMPLE 1.1; 100 mg, 0.25 mmol) in dry acetonitrile (CH3CN) (10 mL) was added Cs2CO3 (162 mg, 0.5 mmol). The reaction mixture was cooled to 0° C. with an ice bath, and iodomethane (70 mg, 0.50 mmol) was added dropwise to the reaction mixture. 1 hour later, the reaction mixture was warmed to RT, and stirred overnight. Then the reaction mixture was washed with brine, dried over Na2SO4, filtered, and concentrated under vacuum to give the crude product. The crude product was purified via flash chromatography on silica gel (20% to 45% EtOAc in petroleum ether) to give 2-(4-((3-(4-methoxypiperidin-1-yl)pyrazin-2-yl)oxy)piperidin-1-yl)quinoline (81 mg, 0.19 mmol, 78% yield) as a white solid. ESI-MS (M+1): 420 calc. for C24H29N5O2 419.

후처리

  1. temperature1 hour later, the reaction mixture was warmed to RT
  2. washThen the reaction mixture was washed with brine
  3. dry with materialdried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated under vacuum
  6. customto give the crude product
  7. customThe crude product was purified via flash chromatography on silica gel (20% to 45% EtOAc in petroleum ether)

출처 및 근거

ORD 기록
ord-81bff78a119d46fc91fdbb1aef46780e
출처 데이터셋
uspto-grants-2016_06
특허 번호
US09376450B2

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