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Triethylamine → HCID 178495911, Verbindung

HRID 747542
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 747542
[CH3:1][O:2][CH2:3][CH2:4][NH:5][C:6]1[C:7]([CH3:19])=[C:8]([CH:12]=[CH:13][C:14]=1[S:15]([CH3:18])(=[O:17])=[O:16])[C:9]([OH:11])=O.[OH:20][C:21]1[N:25]([CH3:26])[N:24]=[C:23]([CH:27]2[CH2:29][CH2:28]2)[CH:22]=1.[CH3:30]CN=C=NCCCN(C)C.CCN(CC)CC.[Si](C#N)(C)(C)C.[C-]#N.[K+]>CC#N>[CH:27]1([C:23]2[C:22]([C:9]([C:8]3[CH:12]=[CH:13][C:14]([S:15]([CH3:18])(=[O:17])=[O:16])=[C:6]([N:5]([CH2:4][CH2:3][O:2][CH3:1])[CH3:30])[C:7]=3[CH3:19])=[O:11])=[C:21]([OH:20])[N:25]([CH3:26])[N:24]=2)[CH2:29][CH2:28]1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 6

HCID 8471TriethylamineHCID 9032Potassium CyanideHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 82115Trimethylsilyl cyanideHCID 691167263-[(2-Methoxyethyl)amino]-2-methyl-4-(methylsulfonyl)benzoic acidHCID 178481725HCID 178481725, Verbindung

Produkt 1

HCID 178495911HCID 178495911, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6342AcetonitrileLösungsmittel

Versuchsvorschrift

Under nitrogen, 0.59 g of crude 3-[(2-methoxyethyl)amino]-2-methyl-4-(methylsulfonyl)benzoic acid was dissolved in 30 ml of CH3CN, and 0.35 g (3 mmol) of 5-hydroxy-3-cyclopropyl-1-methylpyrazole and 0.45 g (2 mmol) of EDAC were then added. The mixture was stirred at RT for one day. 0.36 g (4 mmol) of NEt3, 0.08 g (1 mmol) of Me3SiCN and a spatula tip of KCN were then added, and the mixture was stirred at RT for two days. The mixture was then concentrated, and the residue was taken up in 100 ml of CH2Cl2 and washed with 10% strength H2SO4. The organic phase was dried over MgSO4, concentrated and the residue was purified chromatographically (SiO2, EA/n-heptane=1:1+5% acetic acid). This gave a brown oil.

Aufarbeitung

  1. stirringthe mixture was stirred at RT for two days
  2. concentrationThe mixture was then concentrated
  3. washwashed with 10% strength H2SO4
  4. dry with materialThe organic phase was dried over MgSO4
  5. concentrationconcentrated
  6. customthe residue was purified chromatographically (SiO2, EA/n-heptane=1:1+5% acetic acid)
  7. customThis gave a brown oil

Quellen und Nachweise

ORD-Eintrag
ord-2efd1ae87ab44b23846c95781fa36380
Quelldatensatz
uspto-grants-2008_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US07396939B2

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