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Azidotrimethylsilane → HCID 178491865, Verbindung

HRID 1614874
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1614874
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH:10][C@H:11]2[CH2:15][CH2:14][C@@H:13]([C:16]3[CH:23]=[CH:22][C:19]([C:20]#[N:21])=[CH:18][CH:17]=3)[CH2:12]2)[CH3:9])=[CH:4][C:3]=1[O:24][CH3:25].C[Si]([N:30]=[N+:31]=[N-:32])(C)C>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C@H:8]([NH:10][C@H:11]2[CH2:15][CH2:14][C@@H:13]([C:16]3[CH:17]=[CH:18][C:19]([C:20]4[NH:32][N:31]=[N:30][N:21]=4)=[CH:22][CH:23]=3)[CH2:12]2)[CH3:9])=[CH:4][C:3]=1[O:24][CH3:25]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

4

Edukt 2

HCID 78378AzidotrimethylsilaneHCID 687501784-[(1R,3S)-3-[[(1R)-1-(4-fluoro-3-methoxy-phenyl)ethyl]amino]cyclopentyl]benzonitrile

Produkt 1

HCID 178491865HCID 178491865, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Reaktionsbedingungen

Temperatur
118 °C

Versuchsvorschrift

4-[(1R,3S)-3-[[(1R)-1-(4-fluoro-3-methoxy-phenyl)ethyl]amino]cyclopentyl]benzonitrile (5.1 g, 14.4 mmol) in toluene (160 ml) was treated with trimethylsilylazide (9.5 ml, 72 mmol, dropwise addition) followed by SnBu2O (717 mg, 2.88 mmol). The reaction mixture was stirred at 118° C. overnight. The precipitate was filtered off, and the filtrate was evaporated and purified by flash chromatography (gradient of 0-10%, MeOH in DCM containing 2% NEt3). The product thus obtained was precipitated from EtOH, redissolved in DCM and extracted with aqueous HCl (pH 1). The aqueous phase was neutralized to pH 5-6 with NaOH aq. (1M), and the resulting precipitate was filtered off and dried to afford the title compound. 1H NMR (300 MHz, DMSO) δ 7.89 (d, J=8.2 Hz, 2H), 7.39 (dd, J=8.3, 1.8 Hz, 1H), 7.33-7.23 (m, 3H), 7.14-7.03 (m, 1H), 4.38 (q, J=6.5 Hz, 1H), 3.86 (s, 3H), 3.45-3.32 (m, 1H), 3.09-2.95 (m, 1H), 2.38-2.25 (m, 1H), 2.10-1.64 (m, 5H), 1.56 (d, J=6.7 Hz, 3H).

Aufarbeitung

  1. addition9.5 ml, 72 mmol, dropwise addition)
  2. filtrationThe precipitate was filtered off
  3. customthe filtrate was evaporated
  4. custompurified by flash chromatography (gradient of 0-10%, MeOH in DCM containing 2% NEt3)
  5. customThe product thus obtained
  6. customwas precipitated from EtOH
  7. dissolutionredissolved in DCM
  8. extractionextracted with aqueous HCl (pH 1)
  9. filtrationthe resulting precipitate was filtered off
  10. customdried

Quellen und Nachweise

ORD-Eintrag
ord-3fd69901f4b94502a1650e0fd362ad83
Quelldatensatz
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08765676B2

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