Reaktion #1009764

ord-2c9b8e943a9c40038517396a17c26fc1

Reaktionsgleichung

O
Water
Clc1cc(Br)cc2[nH]ncc12
6-bromo-4-chloro-1H-indazole
O.[Cs+].[OH-]
cesium hydroxide monohydrate
CI
methyl iodide
Cn1ncc2c(Cl)cc(Br)cc21
6-Bromo-4-chloro-1-methyl-1H-indazole
Ausbeute 62.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe aqueous layer was extracted with EtOAc
  2. 2
    EinengenThe organic layer was concentrated
  3. 3
    Sonstigethe crude reside was purified by silica gel column chromatography (EtOAc/Heptane 0 to 100% gradient as eluent)

Vorschrift

To a mixture of 6-bromo-4-chloro-1H-indazole (4.0 g, 17.4 mmol), cesium hydroxide monohydrate (23.3 g, 139 mmol), tetrabutylammonium hydrogensulfate (1.36 g, 3.99 mmol) in anhydrous THF (80 mL) was added a solution of methyl iodide (9.86 g, 69.4 mmol) in THF (10 mL) dropwise at r.t. The reaction mixture was stirred for 15 min at r.t. Water was added to the reaction mixture, and the aqueous layer was extracted with EtOAc. The organic layer was concentrated, and the crude reside was purified by silica gel column chromatography (EtOAc/Heptane 0 to 100% gradient as eluent) to afford 6-Bromo-4-chloro-1-methyl-1H-indazole (2.65 g, 62%). 1H NMR (600 MHz, methanol-d4) δ 4.05 (s, 3H), 7.32 (d, 1H), 7.79 (s, 1H), 8.03 (s, 1H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US09278953B2uspto-grants-2016_03