反应详情

To a solution of 1,1-dimethylethyl 6-[3-(aminocarbonyl)phenyl]-3,4-dihydro-2(1H)-isoquinolinecarboxylate (0.725 g; 2.20 mmol; I-VII-9) and Et3SiH (0.88 mL; 5.5 mmol) in CH2Cl2 (25 mL) at room temperature was added TFA (10 mL) in one portion. The mixture was aged 3 h and concentrated in vacuo (2×PhMe chase). The residue was partitioned between satd Na2CO3/CHCl3 (Note 1), layers were separated and the aqueous layer was extracted with CHCl3 (×4). Combined organics were washed (water, brine), dried over Na2SO4 and concentrated in vacuo, affording the title compound as a colorless solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 2.76 (t, J=5.7 Hz, 2 H), 2.96 (t, J=5.8 Hz, 2 H), 3.87 (s, 2 H), 7.11 (d, J=7.9 Hz, 1 H), 7.40-7.48 (m, 3 H), 7.51 (t, J=7.8 Hz, 1 H), 7.78 (ddd, J=7.7, 1.8, 1.1 Hz, 1 H), 7.82 (ddd, J=7.8, 1.4, 1.3 Hz, 1 H), 8.10 (s, 1 H), 8.12 (t, J=1.6 Hz, 1 H).

1. concentrationconcentrated in vacuo (2×PhMe chase)
2. customThe residue was partitioned between satd Na2CO3/CHCl3 (Note 1), layers
3. customwere separated
4. extractionthe aqueous layer was extracted with CHCl3 (×4)
5. washCombined organics were washed (water, brine)
6. dry with materialdried over Na2SO4
7. concentrationconcentrated in vacuo