Hydrochloric Acid → HCID 69550750, Verbindung

Iodotrimethylsilane (2.51 ml) was added to a solution of 1-[4-benzyloxycarbonylamino-1-(4-pyridyl)-4-piperidylmethyl]-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinone (4.58 g) in dichloromethane (50 ml), and the mixture was stirred at room temperature for 4 hours. Methanol (10 ml) and 4N hydrochloric acid solution in ethyl acetate (8 ml) were added thereto. Methanol was added to obtain a solution, followed by concentration under reduced pressure. Dilute hydrochloric acid was added to the residue, and the mixture was washed with ether. The aqueous layer was made basic with 6N sodium hydroxide, followed by extraction with ethyl acetate. The organic layer was washed successively with an aqueous sodium bicarbonate solution and an aqueous saturated sodium chloride solution, dried, and concentrated. Dilute hydrochloric solution was added to the residue, which was purified by CHP20 column chromatography (water:acetonitrile:1N hydrochloric acid=100:0:1→80:20:1) to obtain the colorless amorphous title compound (3.66 g).

1. customto obtain a solution
2. concentrationfollowed by concentration under reduced pressure
3. additionDilute hydrochloric acid was added to the residue
4. washthe mixture was washed with ether
5. extractionfollowed by extraction with ethyl acetate
6. washThe organic layer was washed successively with an aqueous sodium bicarbonate solution
7. dry with materialan aqueous saturated sodium chloride solution, dried
8. concentrationconcentrated
9. additionDilute hydrochloric solution
10. additionwas added to the residue, which
11. customwas purified by CHP20 column chromatography (water:acetonitrile:1N hydrochloric acid=100:0:1→80:20:1)

ORD-Eintrag

ord-b4d79b17acc44b0a81147ae01c2355ae

Quelldatensatz

uspto-grants-2006_09

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US07109200B2