Tyrosine Kinase Inhibitors
The present disclosure provides compounds that are tyrosine kinase inhibitors, in particular Bruton tyrosine kinase (“BTK”) inhibitors, and are therefore useful for the treatment of diseases treatable by inhibition of BTK such as cancer, autoimmune, inflammatory, and thromboembolic diseases. Also provided are pharmaceutical compositions containing such compounds and processes for preparing such compounds.
1 .- 51 . (canceled)
52 . A method of preparing a compound:
comprising:
reacting a compound:
with an acid in an organic solvent to form the compound:
53 . The method of claim 52 , wherein the acid is trifluoroacetic acid, phosphoric acid, sulfuric acid, or hydrochloric acid.
54 . The method of claim 52 , wherein the acid is hydrochloric acid.
55 . The method of claim 52 , wherein the organic solvent is methanol, ethanol, dichloromethane, acetonitrile, ethyl acetate, tetrahydrofuran, 2-methyltetrahydrofuran, dioxane, tert-butyl methyl ether, cyclopentyl methyl ether, chloroform, or a mixture thereof.
56 . The method of claim 52 , wherein the organic solvent is dioxane.
57 . The method of claim 52 , wherein the compound:
is prepared by reacting a compound:
with a compound:
in a solution comprising a base, an oxidizing agent, a catalyst, and an organic solvent to form the compound:
58 . The method of claim 57 , wherein the base is diisopropylethylamine (DIEA), diisopropylethylamine (DIPEA), N-methylmorpholine (NMM), diethanolamine, pyridine, or triethylamine (TEA).
59 . The method of claim 57 , wherein the base is triethylamine (TEA).
60 . The method of claim 57 , wherein the oxidizing agent is 2-azaadamantane N-oxyl (AZADO), 9-azabicyclo[3.3.1]nonane N-oxyl (ABNO), 4-hydroxy-TEMPO (TEMPOL), 2,2,6,6-tetramethylpiperidine N-oxyl (TEMPO), or oxygen.
61 . The method of claim 57 , wherein the oxidizing agent is 2,2,6,6-tetramethylpiperidine N-oxyl (TEMPO).
62 . The method of claim 57 , wherein the catalyst comprises copper (I) trifuloromethanesulfonate, copper (I) chloride, copper (I) iodide, or copper (II) acetate
63 . The method of claim 57 , wherein the catalyst comprises copper (II) acetate.
64 . The method of claim 57 , wherein the organic solvent is methanol, ethanol, dichloromethane, acetonitrile, ethyl acetate, tetrahydrofuran, 2-methyltetrahydrofuran, dioxane, tert-butyl methyl ether, cyclopentyl methyl ether, chloroform, or a mixture thereof.
65 . The method of claim 57 , wherein the organic solvent is dichloromethane.
66 . The method of claim 57 , wherein the compound:
is prepared by reacting a compound:
with dimethylformamide dimethyl acetal (DMF-DMA) to form the compound:
67 . A method of preparing a compound:
comprising:
reacting a compound:
with a compound:
in a solution comprising a base, an oxidizing agent, a catalyst, and an organic solvent to form the compound:
68 . A method of preparing a compound:
comprising reacting a compound:
with dimethylformamide dimethyl acetal (DMF-DMA) to form the compound: