反应 #1876862
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openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US09056859B2
反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: [4-(1H-Tetrazol-1-yl)phenyl]acetic acid (303 mg, 1.48 mmol) was combined with benzyl 2,5-diazabicyclo[2.2.1]heptane-2-carboxylate (399 mg, 1.48 mmol), EDC (341 mg, 1.78 mmol), and triethylamine (0.248 mL, 1.78 mmol) in DCM (30 mL) and stirred overnight at room temperature. The mixture was washed with 1 M HCl solution, saturated sodium bicarbonate solution, and brine. The organic layer was dried over MgSO4, filtered and concentrated. The crude product was purified by MPLC eluting with a 0-5% gradient of methanol in ethyl acetate to afford benzyl 5-{[4-(1H-tetrazol-1-yl)phenyl]acetyl}-2,5-diazabicyclo[2.2.1]heptane-2-carboxylate. LC/MS: [(M+1)]+=419; The mixture was washed with 1 M HCl solution, saturated sodium bicarbonate solution, and brine The organic layer was dried over MgSO4 filtered concentrated The crude product was purified by MPLC eluting with a 0-5% gradient of methanol in ethyl acetate
来源 ID: ord-7e7cc37e434f4c9ea04bcec500c5b959