Propylamine → HCID 178446867, Verbindung

HRID 892124Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 892124
Cl.[CH2:2]([C@@H:9]1[CH2:20][N:19]2[C:11]([C:12]3[NH:13][C:14]([CH:26]4[CH2:30][CH2:29][CH2:28][CH2:27]4)=[N:15][C:16]=3[N:17]([CH2:22][C:23]([OH:25])=O)[C:18]2=[O:21])=[N:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.[CH2:31](N)[CH2:32][CH3:33].Cl.C([N:38]=C=NCCCN(C)C)C>O.O1CCOCC1>[CH2:2]([C@@H:9]1[CH2:20][N:19]2[C:11]([C:12]3[NH:13][C:14]([CH:26]4[CH2:30][CH2:29][CH2:28][CH2:27]4)=[N:15][C:16]=3[N:17]([CH:22]([CH2:31][CH2:32][CH3:33])[C:23]([NH2:38])=[O:25])[C:18]2=[O:21])=[N:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1

Komponenten

6

Versuchsvorschrift

Compound 77(50 mg, 0.127 mmol) obtained in Example 77 was dissolved in water (1 mL) and 1,4-dioxane (1 mL), to the solution were added n-propylamine (14 μL, 0.176 mmol, 1.4 equivalents) and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (24 mg, 0.127 mmol, 1.0 equivalent), and the mixture was stirred at room temperature for 4 days. The reaction solution was extracted with chloroform, and the extract was washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography (chloroform:methanol=98:2 to 90:10) to obtain the title compound (25 mg, 45%).

Aufarbeitung

  1. extractionThe reaction solution was extracted with chloroform
  2. washthe extract was washed with saturated aqueous sodium chloride
  3. dry with materialdried over anhydrous magnesium sulfate
  4. concentrationconcentrated
  5. customThe residue was purified by silica gel column chromatography (chloroform:methanol=98:2 to 90:10)

Quellen und Nachweise

ORD-Eintrag
ord-f50ee8462e3d45f49e3848992852fd6d
Quelldatensatz
uspto-grants-2006_02
Patentnummer
US07005430B2

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