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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
ノート
印刷プレビュー

反応式

HRID 706728 の反応式
[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]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 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

生成物 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
収率 15%

試薬・触媒・溶媒 2

HCID 962Water溶媒2 回HCID 13387N-methyl-2-pyrrolidone溶媒

反応条件

温度
0 °C

実験手順

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).

後処理

  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

出典と根拠

ORDレコード
ord-61d87a464aa547fb84ef8601f2b5be68
出典データセット
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09174981B2

反応ノート

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