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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120108Generated: October 31, 2026

Methyl iodide → 5-Bromo-2-(1-methyl-1H-tetrazol-5-yl)pyridine

https://huagongshe.com/reaction/2120108

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium HydroxideHCID 14797—
Reactant5-Bromo-2-(2H-tetrazol-5-yl)pyridineHCID 23438683—
SolventDimethylformamideHCID 6228—
Product5-Bromo-2-(1-methyl-1H-tetrazol-5-yl)pyridineHCID 2343856725.9%

Reaction Steps

In 5 ml of dimethylformamide was dissolved 400 mg of 2-(5-tetrazolyl)-5-bromopyridine and the solution was reacted with 502 mg of iodomethane in the presence of 300 mg of potassium hydroxide at room temperature for 1 hour with stirring. After completion of the reaction, a post-treatment similar to that of Preparation Example 3 was conducted to obtain 110 mg of 2-(1-methyl-5-tetrazolyl)-5-bromopyridine (thin layer chromatography eluting with a mixture of 1:4 ethyl acetate:hexane, Rf: 0.3) and 220 mg of 2-(2-methyl-5-tetrazolyl)-5-bromopyridine (thin layer chromatography eluting with a mixture of 1:4 ethyl acetate:hexane, Rf: 0.5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689779B2
Source datasetuspto-grants-2004_02
ORD IDord-214a21cf4c9548b486a95f4e2783055d
Source noteuspto-grants-2004_02