반응 #319159

ord-acefb080ef4b44a189946b513d6dc3ae

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    여과filtration
  2. 2
    세척the residue was washed with water (2×20ml)
  3. 3
    건조with ether (1×20ml) and suction-dried

실험 절차

By the procedure of Example 4, 0.3 g of the sulfonamide prepared in Example 3 was reacted with 0.29 g of phenyl(4-methoxy-6-methyl-1,3,5-triazin-2-yl)carbamate and 0.15 g of "DBU" in 10 ml of p-dioxane. After stirring two hours at room temperature the solution was diluted with about 75 ml of water and acidified with concentrated hydrochloric acid (red to litmus paper). Following filtration, the residue was washed with water (2×20ml) then with ether (1×20ml) and suction-dried to give 0.15 g of the subject compound; m.p. 140°-146° C. NMR (CDCl3): δ2.6(d,6H,SCH3, OCH3); 4.1 (S, 3H, CH3); 4.9(S, 2H, CH2); 7.4-7.7(m, 4H, Ar+NH); 8.3(d, 1H, Ar).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US04851030uspto-grants-1989_07