Bcl-2 protein apoptosis inducer and application
A general formula, stereoisomer technology, applied in the field of immunity and autoimmune diseases, can solve the problem of reducing the efficacy of BCL-2 inhibitors
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Embodiment 1
[0403] Example 1: (S)-2-((1H-pyrrolo[2,3-b]pyridin-5-yl)oxy)-4-(2-(2-(2-isopropylphenyl) Pyrrolidin-1-yl)-7-azaspiro[3.5]nonan-7-yl)-N-((5-nitro-2H,4H-spiro[benzo[b][1,4] Oxazine-3,1'-cyclopropane]-7-yl)sulfonyl)benzamide (001)
[0404]
[0405] Step 1, Dissolve (S)-2-(2-bromophenyl)pyrrolidine-1-carboxylate tert-butyl ester (4.5 g) and isopropylboronic acid (3.1 g) in 15 mL of 1,4-epoxyhexa In the mixed solvent of ring and 3mL water, under nitrogen protection, add potassium carbonate (6g) and Pd(dffp) 2 Cl 2 (0.9g), heated to reflux overnight. TLC monitoring, after the reaction was completed, it was lowered to room temperature, ethyl acetate was added, washed with water and saturated brine respectively, the organic phase was separated and dried with anhydrous sodium sulfate, filtered, the filtrate was concentrated under reduced pressure, and the obtained crude product was purified by silica gel column chromatography to obtain the product (S)-tert-butyl 2-(2-isopropylph...
Embodiment 2
[0416] Example 2: (S)-3-((1H-pyrrolo[2,3-b]pyridin-5-yl)oxy)-5-(2-(2-(2-isopropylphenyl) Pyrrolidin-1-yl)-7-azaspiro[3.5]nonan-7-yl)-N-((5-nitro-2H,4H-spiro[benzo[b][1,4] Oxazine-3,1'-cyclopropane]-7-yl)sulfonyl)pyridinamide (002)
[0417]
[0418] The synthetic method of parameter embodiment 1, replace methyl 2,4-difluorobenzoate with methyl 3,5-difluoropyridine-2-carboxylate, can synthesize target compound (S)-3-((1H- Pyrrolo[2,3-b]pyridin-5-yl)oxy)-5-(2-(2-(2-isopropylphenyl)pyrrolidin-1-yl)-7-azaspiro[ 3.5] Nonan-7-yl)-N-((5-nitro-2H,4H-spiro[benzo[b][1,4]oxazine-3,1'-cyclopropane]-7- yl)sulfonyl)pyridinamide (90mg), LC-MS (ESI-MS): 833[M+H] + .
Embodiment 3
[0419] Example 3: (S)-2-((1H-pyrrolo[2,3-b]pyridin-5-yl)oxy)-3-fluoro-4-(2-(2-(2-isopropyl ylphenyl)pyrrolidin-1-yl)-7-azaspiro[3.5]nonan-7-yl)-N-((5-nitro-2H,4H-spiro[benzo[b][ 1,4]oxazine-3,1'-cyclopropane]-7-yl)sulfonyl)benzamide (003)
[0420]
[0421] The synthetic method of parameter embodiment 1, replace methyl 2,4-difluorobenzoate with methyl 2,3,4 trifluorobenzoate, can synthesize target compound (S)-2-((1H-pyrrolo [2,3-b]pyridin-5-yl)oxy)-3-fluoro-4-(2-(2-(2-isopropylphenyl)pyrrolidin-1-yl)-7-aza Spiro[3.5]nonan-7-yl)-N-((5-nitro-2H,4H-spiro[benzo[b][1,4]oxazine-3,1'-cyclopropane]- 7-yl)sulfonyl)benzamide (66mg), LC-MS (ESI-MS): 850[M+H] + .
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