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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446236Generated: October 29, 2026

7-iodo-3-isobutyl-3H-benzoimidazole-5-carboxylic acid methyl ester → 3-Isobutyl-7-(5-methyl-pyridin-2-yl)-3H-benzoimidazole-5-carboxylic acid methyl ester

https://huagongshe.com/reaction/446236

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-iodo-3-isobutyl-3H-benzoimidazole-5-carboxylic acid methyl esterHCID 59627773—
ReactantHCID 178427808HCID 178427808—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product3-Isobutyl-7-(5-methyl-pyridin-2-yl)-3H-benzoimidazole-5-carboxylic acid methyl esterHCID 5962776457.2%

Reaction Steps

To a solution of 7-iodo-3-isobutyl-3H-benzoimidazole-5-carboxylic acid methyl ester (400 mg, 1.12 mmol) in THF (4 mL) was added Pd(PPh3)4 (65 mg, 0.056 mmol), followed by 5-methyl-pyridinyl zinc bromide (2.68 mL of 0.5M solution in THF, 1.34 mmol). The reaction mixture was stirred overnight at room temperature, then quenched by addition of saturated aqueous NH4Cl solution. The mixture was partitioned between water and ethyl acetate, and the organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure. Purification by column chromatography gave 207 mg (57%) of 3-Isobutyl-7-(5-methyl-pyridin-2-yl)-3H-benzoimidazole-5-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476457B2
Source datasetuspto-grants-2013_07
ORD IDord-3904f1a2f84f4933b5edd15f24e473d3
Source noteuspto-grants-2013_07