4-Methylmorpholine → Boc-DTrp-DNle-OtBu

HRID 977522

Reaktionsgleichung

Reaktionsgleichung von HRID 977522
[NH2:1][C@@H:2]([C:7]([O:9][C:10]([CH3:13])([CH3:12])[CH3:11])=[O:8])[CH2:3][CH2:4][CH2:5][CH3:6].Cl.CN1CCOCC1.[NH:22]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[C@@H:23]([C:34](O)=[O:35])[CH2:24][C:25]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[NH:27][CH:26]=1.C1C=CC2N(O)N=NC=2C=1.CCN=C=NCCCN(C)C.Cl>ClCCl.C(OCC)(=O)C.O>[NH:22]([C:37]([O:39][C:40]([CH3:43])([CH3:42])[CH3:41])=[O:38])[C@@H:23]([C:34]([NH:1][C@@H:2]([C:7]([O:9][C:10]([CH3:12])([CH3:11])[CH3:13])=[O:8])[CH2:3][CH2:4][CH2:5][CH3:6])=[O:35])[CH2:24][C:25]1[C:33]2[C:28](=[CH:29][CH:30]=[CH:31][CH:32]=2)[NH:27][CH:26]=1

Komponenten

9

Edukt 5

HCID 79724-MethylmorpholineHCID 757711-HydroxybenzotriazoleHCID 111050N-((tert-Butoxy)carbonyl)-D-tryptophanHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 131719304tert-butyl (2R)-2-aminohexanoate hydrochloride

Produkt 1

HCID 131719303Boc-DTrp-DNle-OtBuAusbeute 95,6 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittelHCID 8857Ethyl AcetateLösungsmittel

Versuchsvorschrift

To a suspension of H-DNle-OtBu.HCl (603 mg) in dichloromethane (10 ml) were added NMM (297 μl), Boc-DTrp-OH (903 mg), HOBT.H2O (413 mg) and EDCI.HCl (569 mg) successively under ice cooling. The mixture was stirred at the same temperature for 2 h and at room temperature for 1 h. The reaction mixture was diluted with ethyl acetate, washed with 10% aq. citric acid, sat. aq. NaHCO3, water and brine successively, dried over MgSO4 and evaporated in vacuo to give Boc-DTrp-DNle-OtBu (1.22 g). To a solution of the dipeptide derivative in dichloromethane (12 ml) were added methyl chloroformate (1 ml), pulverized NaOH (103 mg) and TBAHS (20 mg). After being stirred of the mixture at room temperature for 30 min, pulverized NaOH (103 mg) was added. This procedure was repeated twice more. The reaction mixture was diluted with dichloromethane, washed with sat. aq. NaHCO3, 10% aq. citric acid, water and brine successively, dried over MgSO4 and evaporated in vacuo. The residue was recrystallized from ethyl acetate and hexane to give Boc-DTrp(COOMe)-DNle-OtBu (1.15 g). The dipeptide derivative (1.03 g) was dissolved in TFA (10 ml) and the solution was stirred under ice cooling for 10 min. After evaporation of the reaction mixture, the residue was dissolved in ethyl acetate. The solution was washed with sat. aq NaHCO3, water and brine successively, dried over MgSO4 and concentrated under reduced pressure to give H-DTrp(COOMe)-DNle-OtBu as a free base. To a solution of the free base (750 mg) in methanol was added 3.78N - hydrogen chloride/1,4-dioxane (0.47 ml) under ice cooling. The solution was evaporated in vacuo to give H-DTrp(COOMe)-DNle-OtBu.HCl (810 mg).

Aufarbeitung

  1. washwashed with 10% aq. citric acid, sat. aq. NaHCO3, water and brine successively
  2. dry with materialdried over MgSO4
  3. customevaporated in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-9669a859c735446ebd7aa2a5276a0e6d
Quelldatensatz
uspto-grants-1997_03
Patentnummer
US05614498

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