4-Methylmorpholine → N-(t-butyloxy)-2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-6-(N,N-dimethylamino) hexanamide

HRID 1720593

Reaktionsgleichung

Reaktionsgleichung von HRID 1720593
[Li+].[CH3:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([S:10]([N:13]([CH2:25][C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C@H:14]([CH2:18][CH2:19][CH2:20][CH2:21][N:22]([CH3:24])[CH3:23])[C:15]([O-])=[O:16])(=[O:12])=[O:11])=[CH:6][CH:5]=1.CN1CCOCC1.O.ON1C2C=CC=CC=2N=N1.Cl.[C:51]([O:55][NH2:56])([CH3:54])([CH3:53])[CH3:52].Cl.CN(CCCN=C=NCC)C>C(Cl)Cl>[C:51]([O:55][NH:56][C:15](=[O:16])[C@H:14]([N:13]([S:10]([C:7]1[CH:8]=[CH:9][C:4]([O:3][CH3:2])=[CH:5][CH:6]=1)(=[O:12])=[O:11])[CH2:25][C:26]1[CH:27]=[CH:28][CH:29]=[CH:30][CH:31]=1)[CH2:18][CH2:19][CH2:20][CH2:21][N:22]([CH3:23])[CH3:24])([CH3:54])([CH3:53])[CH3:52]

Komponenten

7

Versuchsvorschrift

To a solution of 2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-6-(N,N-dimethylamino) hexanoic acid lithium salt (4.42 g, 10.18 mmol) in methylene chloride (100 mL) containing N-methylmorpholine (6.73 mL, 61.06 mmol), 1-hydroxybenzotriazole monohydrate (1.64 g, 10.687 mmol) and O-t-butylhydroxyl amine hydrochloride (1.41 g, 11.20 mmol) is added N-[dimethylaminopropyl]-N'-ethylcarbodiimide hydrochloride (3.90 g, 20.36 mmol) at 0° C. The reaction mixture is allowed to warm to room temperature and stirring is continued overnight. The mixture is diluted with methylene chloride, washed with saturated sodium bicarbonate, then with brine, dried (Na2SO4) and the solvent is evaporated. The crude product is purified by silica gel chromatography (10:1:0.5 ethyl acetate/methanol/ammonium hydroxide) to provide N-(t-butyloxy)-2(R)-[[4-methoxybenzenesulfonyl](benzyl)amino]-6-(N,N-dimethylamino) hexanamide.

Aufarbeitung

  1. washwashed with saturated sodium bicarbonate
  2. dry with materialwith brine, dried (Na2SO4)
  3. customthe solvent is evaporated
  4. customThe crude product is purified by silica gel chromatography (10:1:0.5 ethyl acetate/methanol/ammonium hydroxide)

Quellen und Nachweise

ORD-Eintrag
ord-363a7ad8bd164a84a7d3ea3be34c99c8
Quelldatensatz
uspto-grants-1996_04
Patentnummer
US05506242

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