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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490091Generated: October 30, 2026

Water → 5-cyano-N-(4-methoxybenzyl)-3-methylindazole

https://huagongshe.com/reaction/490091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantEthyl AcetateHCID 8857—
ReactantSodium CyanideHCID 8929—
Reactant5-bromo-N-(4-methoxybenzyl)-3-methylindazoleHCID 69000908—
CatalystNickel(II) bromideHCID 278492—
SolventN-methyl-2-pyrrolidoneHCID 13387—
SolventSodium chloride; waterHCID 57417360—
Product5-cyano-N-(4-methoxybenzyl)-3-methylindazoleHCID 6899920899.4%

Reaction Conditions

Temperature180 °C

Reaction Steps

To a solution of 5-bromo-N-(4-methoxybenzyl)-3-methylindazole 105 (0.12 g, 0.363 mmol) in NMP (N-methylpyrrolidinone; 2 mL) was added sodium cyanide (0.035 g, 0.714 mmol) and nickel bromide (0.079 g, 0.362 mmol). The reaction mixture was heated in a microwave reactor at 180° C. for 20 minutes. Ethyl acetate (100 mL) was added and the organic layer was washer with water and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporated under reduced pressure. The crude product was purified by flash column chromatography to yield the desired 5-cyano-N-(4-methoxybenzyl)-3-methylindazole 106 (0.1 g, 0.361 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528132B2
Source datasetuspto-grants-2009_05
ORD IDord-a3228b1610b64aa3881d2ef461f1f1f5
Source noteuspto-grants-2009_05