反应 #4149951
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openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e44c05f55084e8ab7cbb1b0ab728054暂无可渲染的结构数据
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e44c05f55084e8ab7cbb1b0ab728054反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6cf99b729547456796bcad8b996df833反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3a5b4c8628054eeea1fec05807755ac9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-73eadd0e184e41febcaa08285557e221反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f5cd72f7770442e8a6f077e9bd8a216e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-9e44c05f55084e8ab7cbb1b0ab728054反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The title compound was prepared as described in Example 1C, substituting 3-chloro-6-methylpyridazine for 3-bromopyridine and tert-butyl azetidine-3-carboxylate for tert-butyl 4-(4-(azetidine-3-carboxamido)phenoxy)piperidine-1-carboxylate.
来源 ID: ord-9667ead9fee54d1a82f9ae008a6bc595反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-6cf99b729547456796bcad8b996df833反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-3a5b4c8628054eeea1fec05807755ac9反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-73eadd0e184e41febcaa08285557e221反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f5cd72f7770442e8a6f077e9bd8a216e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 3-(4-(bromomethyl)phenyl)-5-(3-(pyridin-2-yl)-4-(trifluoromethyl)-isoxazol-5-yl)-1,2,4-oxadiazole (2.52 g, 5.59 mmol) and tert-butyl azetidine-3-carboxylate, acetic acid (1.82 g, 8.39 mmol) in N,N-dimethylformamide (40 mL) cooled with an ice-water bath was added triethylamine (2.34 mL, 16.8 mmol) drop-wise. The reaction mixture was stirred for 30 minutes, diluted with ethyl acetate (350 mL), washed with a 10% aqueous solution of lithium chloride (2×100 mL), washed with water (100 mL), washed with brine (100 mL), and dried over anhydrous sodium sulfate. Concentration gave a crude product which was triturated with methanol. The resulting solid was collected by vacuum filtration. The filtrate was concentration and purified by silica gel chromatography (eluting with Hexanes/ethyl acetate-4/1) to yield additional product. The material was combined to give tert-butyl 1-(4-(5-(3-(pyridin-2-yl)-4-(trifluoromethyl)isoxazol-5-yl)-1,2,4-oxadiazol-3-yl)benzyl)azetidine-3-carboxylate (2.46 g, 83% yield). washed with a 10% aqueous solution of lithium chloride (2×100 mL) washed with water (100 mL) washed with brine (100 mL) dried over anhydrous sodium sulfate Concentration gave a crude product which was triturated with methanol The resulting solid was collected by vacuum filtration concentration purified by silica gel chromatography (eluting with Hexanes/ethyl acetate-4/1) to yield additional product
来源 ID: ord-af26589c19f14b6cb9ac8d49e2b525dcPubChem References
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