反应详情

To a suspension of 5.16 g (0.02 mol) finely powdered nicotinoyldopamine in 100 ml chloroform, 7.23 g (0.06 mol) trimethylacetyl chloride were added under stirring. The mixture was refluxed for 6 hrs and then filtered. The filtrate was washed with water free of chloride ions, then washed once with a 5% solution of NaHCO3, then with water. The chloroform was evaporated and the residue was chromatographed by using a silica gel G column and 2% methanol in chloroform as the eluent. The first fraction was collected and evaporated and the residue was crystallized from ether/petroleum ether. Yield, 6.2 g (73%) of a white crystalline solid, m.p. 112°-114° C., NMR (CDCl3) δ 9.06 (bs, 1H, C2 pyridine proton), 8.73 (bd, 1H, C6 pyridine proton), 8.30-8.13 (m, 1H, C4 pyridine proton), 7.46-7.10 (m, 5H, C6H3 +C5 pyridine proton + CONH), 3.66 (q, 2H, J=6.25 Hz, --N--CH2), 3.0 (t, 2H, J=6 Hz, --CH2), 1.41 (s, 18H, 2--C(CH3)3). Anal. Calcd for C24H30N2O5 : C, 67.58; H, 7.09; N, 6.56. Found: C, 67.61; H, 7.10; N, 6.54.

1. additionwere added
2. temperatureThe mixture was refluxed for 6 hrs
3. filtrationfiltered
4. washThe filtrate was washed with water free of chloride ions
5. washwashed once with a 5% solution of NaHCO3
6. customThe chloroform was evaporated
7. customthe residue was chromatographed
8. customThe first fraction was collected
9. customevaporated
10. customthe residue was crystallized from ether/petroleum ether
11. customYield