反应详情

A solution of tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylate (100 mg, 0.257 mmol) in 1 mL of CH2Cl2 and 1 mL of TFA was stirred for 1 h and concentrated. The oil was redissolved in 2 mL of CH2Cl2 and treated with NEt3 (0.15 mL, 1.08 mmol) and CbzCl (0.060 mL, 0.42 mmol), then stirred for 8 h. The mixture was partitioned between EtOAc and sat'd NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was stirred in 3 mL of 1:1:1 MeOH/THF/water with LiOH.H2O (30 mg, 0.71 mmol) for 10 h, concentrated to dryness, dissolved in 2 mL of DMF, treated with EDC (150 mg, 0.79 mmol), HOBt (100 mg, 0.74 mmol), and phenylenediamine (100 mg, 0.93 mmol). The mixture was stirred for 18 h, concentrated, and triturated with methanol giving the title compound; MS (ESI+): cal'd [M+1]+ 500.3, obs'd 500.3.

1. concentrationconcentrated
2. dissolutionThe oil was redissolved in 2 mL of CH2Cl2
3. customThe mixture was partitioned between EtOAc
4. dry with materialdried (Na2SO4)
5. filtrationfiltered
6. concentrationconcentrated
7. concentrationconcentrated to dryness
8. dissolutiondissolved in 2 mL of DMF
9. stirringThe mixture was stirred for 18 h
10. concentrationconcentrated
11. customtriturated with methanol giving the title compound