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Chlorotrimethylsilane → Tert-butyl 3-(4-bromothiazol-2-yl)azetidine-1-carboxylate

HRID 1051591
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1051591
BrCCBr.Cl[Si](C)(C)C.I[CH:11]1[CH2:14][N:13]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:12]1.Br[C:23]1[S:24][CH:25]=[C:26]([Br:28])[N:27]=1>O1CCCC1.[Zn].C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.[Pd].O>[Br:28][C:26]1[N:27]=[C:23]([CH:11]2[CH2:14][N:13]([C:15]([O:17][C:18]([CH3:21])([CH3:20])[CH3:19])=[O:16])[CH2:12]2)[S:24][CH:25]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

9

Edukt 4

HCID 6397ChlorotrimethylsilaneHCID 78391,2-DibromoethaneHCID 27632972,4-Dibromo-1,3-thiazoleHCID 11000522Tert-butyl 3-iodoazetidine-1-carboxylate

Produkt 1

HCID 118076258Tert-butyl 3-(4-bromothiazol-2-yl)azetidine-1-carboxylateAusbeute 15,3 %

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 23994
Zinc
Katalysator
HCID 11979704Tetrakis(triphenylphosphine)palladiumKatalysator
HCID 962WaterLösungsmittel
HCID 8028TetrahydrofuranLösungsmittel4×

Reaktionsbedingungen

Temperatur
80 °C

Versuchsvorschrift

1,2-Dibromoethane (0.084 mL, 0.97 mmol) was added to a mixture of zinc powder (0.520 g, 8.13 mmol) in tetrahydrofuran (2 mL), and the resulting mixture was stirred for 10 min at 80° C. and was then cooled to room temperature. A solution of chlorotrimethylsilane (0.115 mL, 1.22 mmol) in tetrahydrofuran (1 mL) was added dropwise with stirring, and the resulting mixture stirred for 45 min at room temperature. A solution of tert-butyl 3-iodoazetidine-1-carboxylate (1.74 g, 6.15 mmol) in tetrahydrofuran (2 mL) was added, and the resulting mixture stirred for 2 h at room temperature. A solution of 2,4-dibromothiazole (0.744 g, 3.09 mmol) in tetrahydrofuran (1 mL) and tetrakis(triphenylphosphine)palladium(O) (0.354 g, 0.31 mmol) were added, and the resulting mixture stirred overnight at room temperature. The reaction mixture was poured into water (10 mL) and extracted with ethyl acetate (3×10 mL). The combined organic layers were dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum. The residue was purified via column chromatography on silica gel (eluting with 1:2, ethyl acetate/petroleum ether) to afford tert-butyl 3-(4-bromothiazol-2-yl)azetidine-1-carboxylate (0.151 g, 8%) of as yellow oil. MS (ESI, pos. ion) m/z 319, 321 [M+H]+.

Aufarbeitung

  1. temperaturewas then cooled to room temperature
  2. stirringwith stirring
  3. stirringthe resulting mixture stirred for 45 min at room temperature
  4. stirringthe resulting mixture stirred for 2 h at room temperature
  5. stirringthe resulting mixture stirred overnight at room temperature
  6. extractionextracted with ethyl acetate (3×10 mL)
  7. dry with materialThe combined organic layers were dried over anhydrous sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under vacuum
  10. customThe residue was purified via column chromatography on silica gel (eluting with 1:2, ethyl acetate/petroleum ether)

Quellen und Nachweise

ORD-Eintrag
ord-181191102f0c44db8cb1f0510d9a0dbe
Quelldatensatz
uspto-grants-2016_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09388161B2

Notizen zur Reaktion

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