Methylamine → 5-(3-((7-methoxyquinolin-4-yloxy)methyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-N-methylthiophene-2-carboxamide

HRID 40243Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 40243
[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([O:13][CH2:14][C:15]3[N:19]4[CH:20]=[C:21]([C:24]5[S:28][C:27]([C:29](Cl)=[O:30])=[CH:26][CH:25]=5)[CH:22]=[CH:23][C:18]4=[N:17][N:16]=3)=[CH:8][CH:9]=[N:10]2)=[CH:5][CH:4]=1.C[CH2:33][N:34](C(C)C)C(C)C.CN>C(Cl)Cl.C1COCC1>[CH3:1][O:2][C:3]1[CH:12]=[C:11]2[C:6]([C:7]([O:13][CH2:14][C:15]3[N:19]4[CH:20]=[C:21]([C:24]5[S:28][C:27]([C:29]([NH:34][CH3:33])=[O:30])=[CH:26][CH:25]=5)[CH:22]=[CH:23][C:18]4=[N:17][N:16]=3)=[CH:8][CH:9]=[N:10]2)=[CH:5][CH:4]=1

Komponenten

6

Versuchsvorschrift

To a solution of 5-(3-((7-methoxyquinolin-4-yloxy)methyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)thiophene-2-carbonyl chloride (0.150 g, 0.33 mmol) and Hunig's Base (0.17 ml, 1.00 mmol) in DCM (2.5 mL) was added methanamine (0.17 ml, 0.33 mmol) in THF dropwise. The solution was stirred at room temperature for 3 hours, at which point an additional 1.5 equivalents of amine were added. The solution was concentrated in vacuo and purified via flash chromatography eluting with 3-8% MeOH:NH4OH in DCM. There remained an impurity, so the product was triturated with MeCN, filtered and washed with DCM to yield 5-(3-((7-methoxyquinolin-4-yloxy)methyl)-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-N-methylthiophene-2-carboxamide (0.0276 g, 19% yield) as an amorphous tan solid.

Aufarbeitung

  1. additionwere added
  2. concentrationThe solution was concentrated in vacuo
  3. custompurified via flash chromatography
  4. washeluting with 3-8% MeOH
  5. customso the product was triturated with MeCN
  6. filtrationfiltered
  7. washwashed with DCM

Quellen und Nachweise

ORD-Eintrag
ord-c9b4cbbd0333473ca7eded607268e2db
Quelldatensatz
uspto-grants-2013_09
Patentnummer
US08524900B2

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