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Sodium Hydroxide → N-(1-((6-isopropylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

HRID 706728
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HRID 706728 반응식
[CH3:1][N:2]1[CH2:7][CH2:6][N:5]([CH2:8][CH2:9][O:10][C:11]2[CH:16]=[CH:15][N:14]3[C:17]([C:20]([O-])=[O:21])=[CH:18][N:19]=[C:13]3[CH:12]=2)[CH2:4][CH2:3]1.[Li+].ClC1C=C(Cl)C=C(Cl)C=1C(Cl)=O.[CH:36]([C:39]1[N:44]=[C:43]([CH2:45][N:46]2[C:54]3[CH:53]=[CH:52][CH:51]=[C:50]([NH2:55])[C:49]=3[CH:48]=[N:47]2)[CH:42]=[CH:41][CH:40]=1)([CH3:38])[CH3:37].[OH-].[Na+].[NH4+].[Cl-]>O.CN1C(=O)CCC1>[CH:36]([C:39]1[N:44]=[C:43]([CH2:45][N:46]2[C:54]3[C:49](=[C:50]([NH:55][C:20]([C:17]4[N:14]5[CH:15]=[CH:16][C:11]([O:10][CH2:9][CH2:8][N:5]6[CH2:4][CH2:3][N:2]([CH3:1])[CH2:7][CH2:6]6)=[CH:12][C:13]5=[N:19][CH:18]=4)=[O:21])[CH:51]=[CH:52][CH:53]=3)[CH:48]=[N:47]2)[CH:42]=[CH:41][CH:40]=1)([CH3:38])[CH3:37]
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참가 물질

8

반응물 5

HCID 14798Sodium HydroxideHCID 25517Ammonium ChlorideHCID 27337032,4,6-Trichlorobenzoyl chlorideHCID 67252742Lithium 7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxylateHCID 679763201-((6-isopropylpyridin-2-yl)methyl)-1H-indazol-4-amine

생성물 1

HCID 86699346
N-(1-((6-isopropylpyridin-2-yl)methyl)-1H-indazol-4-yl)-7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide
수율 15%

시약·촉매·용매 2

HCID 962Water용매2회HCID 13387N-methyl-2-pyrrolidone용매

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온도
0 °C

실험 절차

To lithium 7-(2-(4-methylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxylate (188 mg, 0.595 mmol) was added NMP (5 mL, distilled over oven dried MgSO4 directly into the 25 mL flask charged with the lithium salt). A heat gun was used to dissolve the starting material. The flask was cooled to 0° C. and 2,4,6-trichlorobenzoyl chloride (94.2 μL, 0.590 mmol) was added drop-wise. The cold bath was removed after addition was complete, and the reaction mixture was stirred for another hour. The reaction mixture turned from a clear solution to slightly cloudy. 1-((6-Isopropylpyridin-2-yl)methyl)-1H-indazol-4-amine (120 mg, 0.451 mmol) was added in one portion to the reaction mixture and the reaction was heated to 88° C. for 5 hours. NMP was removed by a vacuum distillation (at the same bath temperature) until the reaction mixture became a thick oil. NaOH (1.8 mmol) in H2O (10 mL) was added to the thick oil and the solution was stirred at 80° C. for 30 minutes. The solution was cooled to ambient temperature and the pH of the dark solution was adjusted to pH 12 to 13 with saturated NH4Cl. The solution was cooled to 0° C. and H2O (20 mL) was added. Stirring was continued for 30 minutes, during which time solids precipitated out of solution. The mixture was filtered and the filtrate was washed with saturated NaHCO3 and H2O. The resulting solid was dissolved in DCM, dried (Na2SO4), filtered and concentrated. The residue was triturated with MTBE give final product (15%). MS (ES+APCI) m/z=553.1 (M+H).

후처리

  1. distillationdistilled over oven dried MgSO4 directly into the 25 mL flask
  2. additioncharged with the lithium salt)
  3. dissolutionto dissolve the starting material
  4. customThe cold bath was removed
  5. additionafter addition
  6. temperaturethe reaction was heated to 88° C. for 5 hours
  7. customNMP was removed by a vacuum distillation (at the same bath temperature) until the reaction mixture
  8. stirringthe solution was stirred at 80° C. for 30 minutes
  9. temperatureThe solution was cooled to ambient temperature
  10. temperatureThe solution was cooled to 0° C.
  11. stirringStirring
  12. customprecipitated out of solution
  13. filtrationThe mixture was filtered
  14. washthe filtrate was washed with saturated NaHCO3 and H2O
  15. dissolutionThe resulting solid was dissolved in DCM
  16. dry with materialdried (Na2SO4)
  17. filtrationfiltered
  18. concentrationconcentrated
  19. customThe residue was triturated with MTBE

출처 및 근거

ORD 기록
ord-61d87a464aa547fb84ef8601f2b5be68
출처 데이터셋
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09174981B2

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