反应详情

Compound D4 (295 mg, 0.77 mmol) was dissolved in ˜5:1 EtOH:H2O (12 mL), and Fe dust (209 mg)was added. The mixture was vigorously stirred and refluxed for 4 h, and then filtered hot through a pad of Celite. The Celite was washed with boiling EtOH, and EtOH fractions were combined and evaporated to dryness. The residue was extracted into hot water, and filtered through Celite, and then evaporated to dryness. The residue was azeotroped with MeOH (3×20 mL), and then dissolved in MeOH (10 mL). Methanolic HCl (1.25 M, 5 mL) was added, and the solution stirred for 10 min. Solvent was removed under reduced pressure, and the residue was crystallized from MeOH/EtOAc to give D5 (218 mg, 80%); mp (MeOH/EtOAc); 1H NMR [(CD3)2SO] δ11.13 (s, 1 H, NH), 10.44 (s, 1 H, NH), 9.88 (br, 2 H, NH2), 8.36 (d, J=7.5 Hz, 2 H, ArH), 8.12 (d, J=8.6 Hz, 2 H, ArH), 7.86 (d, J=8.8 Hz, 2 H, ArH), 7.50 (d, J=8.8 Hz, 2 H, ArH), 7.32 (d, J=8.6 Hz, 2 H, ArH), 7.32 (d, J=7.5 Hz, 2 H, ArH), 7.30 (d, J=8.7 Hz, 2 H, ArH), 4.00 (s, 3 H, N+CH3); LCMS 319+ve

1. temperaturerefluxed for 4 h
2. filtrationfiltered hot through a pad of Celite
3. washThe Celite was washed with boiling EtOH, and EtOH fractions
4. customevaporated to dryness
5. extractionThe residue was extracted into hot water
6. filtrationfiltered through Celite
7. customevaporated to dryness
8. customThe residue was azeotroped with MeOH (3×20 mL)
9. dissolutiondissolved in MeOH (10 mL)
10. additionMethanolic HCl (1.25 M, 5 mL) was added
11. stirringthe solution stirred for 10 min
12. customSolvent was removed under reduced pressure
13. customthe residue was crystallized from MeOH/EtOAc