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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446229Generated: October 25, 2026

4-iodo-1-isopropyl-1H-indazole-6-carboxylic acid methyl ester → 1-isopropyl-4-(5-methyl-pyridin-2-yl)-1H-indazole-6-carboxylic acid methyl ester

https://huagongshe.com/reaction/446229

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-iodo-1-isopropyl-1H-indazole-6-carboxylic acid methyl esterHCID 59627768—
ReactantHCID 178427808HCID 178427808—
CatalystHCID 178418397HCID 178418397—
SolventTetrahydrofuranHCID 8028—
Product1-isopropyl-4-(5-methyl-pyridin-2-yl)-1H-indazole-6-carboxylic acid methyl esterHCID 5962776550%

Reaction Steps

To a solution of 4-iodo-1-isopropyl-1H-indazole-6-carboxylic acid methyl ester (1.13 g, 3.28 mmol) in THF (30 mL) was added Pd(PPh3)4 (0.2 g, 0.164 mmol), followed by 5-methyl-pyridinyl zinc bromide ((19.7 mL of 0.5M solution in THF, 9.86 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 0.5 g (50%) of 1-isopropyl-4-(5-methyl-pyridin-2-yl)-1H-indazole-6-carboxylic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476457B2
Source datasetuspto-grants-2013_07
ORD IDord-7c652c1b171a4cccb1627b58429f3aa9
Source noteuspto-grants-2013_07