1H-Benzimidazole, 1-methyl- → Tert-butyl 3-(1-methylbenzimidazol-2-yl)azetidine-1-carboxylate

HRID 2418916Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 2418916
CC(C)(C)OC(=O)N1CC(I)C1.Cn1cnc2ccccc21>CS(C)=O.O.O.O=S(=O)(O)O.O=S(=O)(O)O.OO.[Fe]>Cn1c(C2CN(C(=O)OC(C)(C)C)C2)nc2ccccc21

Komponenten

8

Reaktionsbedingungen

Temperatur
25 °C

Versuchsvorschrift

H2O2 (30% in H2O; 0.31 mL, 3.0 mmol) was added to a stirred solution of 1-methylbenzimidazole 1g (100 mg, 1.0 mmol), concentrated H2SO4 (108 μL, 1.0 mmol), 1-Boc-3-(iodo)azetidine (566 mg, 2.0 mmol) and iron(II) sulfate heptahydrate (80 mg, 0.3 mmol) in DMSO (5 mL) at room temperature. The mixture was stirred at room temperature for 120 min, then diluted with EtOAc and saturated NaHCO3. The aqueous and organic layers were partitioned and the organic layer was washed with brine, dried (MgSO4), filtered and the solvent removed under vacuum to leave a crude residue. The residue was purified by column chromatography on silica gel using EtOAc / hexanes (3:7 to 7:3) as eluent to give the desired product 3f(52 mg, 17%) as a solid.

Quellen und Nachweise

ORD-Eintrag
ord-0810a7b8e5134dada871394b3a94393d
Quelldatensatz
Minisci dataset from Roche

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