反应详情

Reduction of this azide to the corresponding amine was carried out according to a published procedure of Gartiser et al., Tetrahedron Lett., 1983, 24:1609. A suspension of 3-azidomethyl-9-(2,5-dichlorobenzyl)-9H-β-carboline (4.60 g, 12 mmol), ammonium formate (3.90 g, 61.7 mmol), and 10% Pd-on-carbon (2.0 g, 20mol %) in ethanol (200 mL) was stirred at room temperature under nitrogen for 15 hours. The reaction mixture was filtered to remove the solids, and the filtrate concentrated and diluted with CH2Cl2 (100 mL). The resulting solution was washed with water (2×25 mL) and brine (25 mL), dried over anhydrous Na2SO4, and concentrated. The crude product was recrystallized from ethyl acetate, affording 3.0 grams (65%) of N-formyl-[9-(2,5-dichlorobenzyl)-9H-β-carbolin-3-yl]methylamine as a pale-yellow solid. 1H NMR (CDCl3) 6 8.65 (s, 1H), 8.30 (s, 1H), 8.24 (d, 1H), 7.95 (s, 1H), 7.58 (t, 7.40 (m, 3H), 7.20 (dd, 1H), 6.51 (s, 1H), 5.60 (s, 2H), 4.78 (d, 1H); MS monoisotopic mass (calculated) 383.1, MH+ (observed) 384.9.

1. filtrationThe reaction mixture was filtered
2. customto remove the solids
3. concentrationthe filtrate concentrated
4. additiondiluted with CH2Cl2 (100 mL)
5. washThe resulting solution was washed with water (2×25 mL) and brine (25 mL)
6. dry with materialdried over anhydrous Na2SO4
7. concentrationconcentrated
8. customThe crude product was recrystallized from ethyl acetate