Compounds and compositions for modulating EGFR mutant kinase activities
A technology of compounds and medicinal salts, applied in the field of compounds and compositions for regulating the kinase activity of EGFR mutants, capable of solving problems such as precise effects, small pleiotropic defects, etc.
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Embodiment 1
[0607] Compound 1: N-(3-(4-(4-(azetidin-1-ylmethyl)-3-methyl-1H-pyrazol-1-yl)pyrimidine-2- (amino)-4-methoxyphenyl)acrylamide
[0608]
[0609] step 1:
[0610] To a solution of Intermediate 1 (35.0 mg, 0.10 mmol), diisopropylethylamine (DIPEA, 50 μL, 0.30 mmol) in dimethylacetamide (DMAA, 2 mL) was added 18.5 mg of the azacycline at room temperature Butane hydrochloride (0.20 mmol). After stirring for 20 minutes, 62.8 mg of sodium triacetoxyborohydride (NaBH(OAc) 3 , 0.30 mmol), and the resulting mixture was stirred at room temperature for 16 hours. The solvent was evaporated in vacuo and the mixture was purified by column chromatography (0 to 10% MeOH in DCM) to afford 4-(4-(azetidin-1-ylmethyl)-3-methyl as a red solid -1H-pyrazol-1-yl)-N-(2-methoxy-5-nitrophenyl)pyrimidin-2-amine (32.0 mg, 82%); MS (ESI) m / z 396.2 [M +H] + .
[0611] Step 2:
[0612] To a solution of the above nitro compound (56.0 mg, 0.14 mmol) in 3 mL of a mixture of ethanol and water (5...
Embodiment 2
[0616] Compound 2: N-(3-(4-(4-((3-hydroxyazetidin-1-yl)methyl)-3-methyl-1H-pyrazol-1-yl) Pyrimidin-2-ylamino)-4-methoxyphenyl)acrylamide
[0617] The title compound was prepared as described in Example 1 using Intermediate 1 and azetidin-3-ol hydrochloride; MS (ESI) m / z 436.2 [M+H] + .
Embodiment 3
[0619] Compound 3: N-(3-(4-(4-(azetidin-1-ylmethyl)-3-methyl-1H-pyrazol-1-yl)pyrimidine-2- Amino)phenyl)acrylamide
[0620] The title compound was prepared as described in Example 1 using Intermediate 2 and azetidine hydrochloride; MS (ESI) m / z 390.2 [M+H] + .
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