Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

5-bromo-3-iodo-1-methyl-1H-indazole synthesis

3synthesis methods
-

Yield:865156-34-9 81 %

Reaction Conditions:

with caesium carbonate in acetonitrile at 20;

Steps:

66.1 Preparation of 5-bromo-3-iodo-1-methyl-1H-indazole

Step1:
Preparation of 5-bromo-3-iodo-1-methyl-1H-indazole. 5-bromo-3-iodo-1H-indazole (2.0 g, 6.2 mmol, 1.0 eq.) was dissolved in acetonitrile (30 mL), CH3I (1.3 g, 9.3 mmol, 1.5 eq.) and Cs2CO3 (3.0 g, 9.3 mmol, 1.5 eq.) were added, and the reaction mixture was stirred at room temperature for 1 h.
The solid was filtered out, the filtrate was rotary evaporated to dryness, and the crude product was purified by column chromatography (PE/EtOAc = 5:1-2:1, gradient elution) to give the title compound as a white solid (1.7 g, yield of 81%). MS (m/z) = 336.88 [M+H]+.

References:

EP4140996,2023,A1 Location in patent:Paragraph 0171; 0172